Wolff rearrangement

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The Wolff rearrangement is a reaction in organic chemistry in which an α-diazocarbonyl compound is converted into a ketene by loss of dinitrogen with accompanying 1,2-rearrangement. The Wolff rearrangement yields a ketene as an intermediate product, which can undergo nucleophilic attack with weakly acidic nucleophiles such as water, alcohols, and amines, to generate carboxylic acid derivatives or undergo [2+2] cycloaddition reactions to form four-membered rings.[1] The mechanism of the Wolff rearrangement has been the subject of debate since its first use. No single mechanism sufficiently describes the reaction, and there are often competing concerted and carbene-mediated pathways; for simplicity, only the textbook, concerted mechanism is shown below.[2] The reaction was discovered by Ludwig Wolff in 1902.[3] The Wolff rearrangement has great synthetic utility due to the accessibility of α-diazocarbonyl compounds, variety of reactions from the ketene intermediate, and stereochemical retention of the migrating group.[2] However, the Wolff rearrangement has limitations due to the highly reactive nature of α-diazocarbonyl compounds, which can undergo a variety of competing reactions.[1]

The Wolff rearrangement and subsequent trapping of the ketene intermediate with a weak acid or olefin.

The Wolff rearrangement can be induced via thermolysis,[3] photolysis,[4] or transition metal catalysis.[3] In this last case, the reaction is sensitive to the transition metal; silver (I) oxide or other Ag(I) catalysts work well and are generally used. The Wolff rearrangement has been used in many total syntheses; the most common use is trapping the ketene intermediate with nucleophiles to form carboxylic acid derivatives. The Arndt-Eistert homologation is a specific example of this use, wherein a carboxylic acid may be elongated by a methylene unit. Another common use is in ring-contraction methods; if the α-diazoketone is cyclic, the Wolff rearrangement results in a ring-contracted product. The Wolff rearrangement works well in generating ring-strained systems, where other reactions may fail.


In 1902, Wolff discovered that treating diazoacetophenone with silver (I) oxide and water resulted in formation of phenylacetic acid. Similarly, treatment with silver (I) oxide and ammonia formed phenylacetamide.[3] A few years later, in an independent study, Schröter observed similar results.[5] The reaction is occasionally called the Wolff-Schröter rearrangement.[2] The Wolff rearrangement was not commonly used until 20 years after it was discovered, as facile diazoketone synthesis was unknown until the 1930s.[2] The reaction has proven useful in synthetic organic chemistry and many reviews have been published.[1][2]

Wolff's original work


The mechanistic pathway of the Wolff-rearrangement has been the subject of much debate, as there are often competing concerted and stepwise mechanisms.[2] However, two aspects of the mechanism can be agreed upon. First, α-diazocarbonyl compounds are in an equilibrium of s-(Z) and s-(E) conformers, the distribution of which may influence the mechanism of the reaction. Generally, under photolysis, compounds in the s-(Z) conformation react stepwise due to the antiperiplanar relationship between the leaving and migrating groups, while compounds in the s-(E) conformation react through a carbene intermediate or do not rearrange. Second, regardless of the reaction mechanism, the rearrangement gives a ketene intermediate, which can be trapped by a weakly acidic nucleophile, such as an alcohol or amine, to give the corresponding ester or amide, or an olefin, to give a [2+2] cycloaddition adduct. Strong acids do not rearrange, but rather protonate the α-carbon and give SN2 products.

Concerted versus stepwise mechanism for ground state conformers.

Stereochemistry of α-diazoketones[edit]

Understanding the stereochemistry of α-diazoketones is essential in elucidating the mechanism of the Wolff rearrangement. α-diazocarbonyl compounds are generally locally planar, with large rotational barriers (55–65 kJ/mol) due to C-C olefin character between the carbonyl and α-carbon, illustrated in the rightmost resonance structure.[6] Such a large barrier slows molecular rotations sufficiently to lead to an equilibrium between two conformers, an s-(E) and s-(Z) conformer. S-(Z) conformers are electronically favored due to Coulombic attraction between the oxygen with a partial negative charge and the cationic nitrogen, as seen in the rightmost resonance structure.[1] If R1 is large and R2 is hydrogen, s-(Z) is sterically favored. If R1 and R2 are large, s-(E) is sterically favored; if both substitents are sufficiently large, the steric repulsion can outweigh the Coulombic attraction, leading to a preference for s-(E). Small and medium cyclic substrates are constrained in the s-(Z) conformation.

Equilibrium between s-(E) and s-(z) with resonance structure showing the olefinic character of the C-C bond, and the Coulombic attraction in s-(Z).

Concerted mechanism[edit]

When the α-diazoketone is in the s-(Z) conformation, the leaving group (N2) and the migrating group (R1) are antiperiplanar, which favors a concerted mechanism, in which nitrogen extrusion occurs concurrently with 1,2-alkyl shift. There is evidence this mechanism occurs in both thermolytic and photolytic methods, when the s-(Z) conformer is strongly favored.[7]

Concerted mechanism from the s-(Z) conformation.

CIDNP studies show that photochemical rearrangement of diazoacetone, which largely exists in the s-(Z) conformer, is concerted.[8] Product ratios from direct and triplet-sensitized photolysis have been used as evidence for proposals that claim that concerted products arise from the s-(Z) conformer and stepwise products occur through the s-(E) conformer.[9]

Stepwise mechanism[edit]

s-(E) α-diazoketones do not have an antiperiplanar relationship between the leaving and migrating group, and thus are thought to generally rearrange stepwise. The stepwise mechanism begins with nitrogen extrusion, forming an α-ketocarbene. The α-ketocarbene can either undergo a 1,2-alkyl shift, to give the ketene product, or can undergo a 4π electrocyclic ring closure, to form an antiaromatic oxirene. This oxirene can reopen in two ways, to either α-ketocarbene, which can then form the ketene product.

Stepwise mechanism from the s-(E) conformation with sequential extrusion of nitrogen to give the ketocarbene, which can either undergo 1,2-alkyl shift to form the carbene or 4π electrocyclic ring closure to give an oxirene intermediate.

There are two primary arguments for stepwise mechanisms. The first is that rate constants of Wolff rearrangements depend on the stability of the formed carbene, rather than the migratory aptitude of the migrating group.[10] The most definitive evidence is isotopic scrambling of the ketene, as predicted by an oxirene intermediate, which can only occur in the stepwise path. In the scheme below, the red carbon is 13C labelled. The symmetric oxirene intermediate can open either way, scrambling the 13C label. If the substituents R1 and R2 are the same, one can quantify the ratio of products stemming from the concerted and stepwise mechanisms; if the substituents are different, the oxirene will have a preference in the direction it opens, and a ratio cannot be quantified, but any scrambling indicates some reactant is going through a stepwise mechanism.[1] In photolysis of diazo acetaldehyde, 8% of the label is scrambled, indicating that 16% of product is formed via the oxirene intermediate.[11] Under photolysis, the biphenyl (R1=R2=phenyl) substrate shows 20–30% label migration, implying 40–60% of product goes through the oxirene intermediate.[12] α-diazocyclohexanone shows no label scrambling under photolytic conditions, as it is entirely s-(Z), and thus all substrate goes through the concerted mechanism, avoiding the oxirene intermediate.[13]

Isotopic scrambling of 13C labeled ketocarbene via symmetric oxirene.

Isotopic labeling studies have been used extensively to measure the ratio of product stemming from a concerted mechanism versus a stepwise mechanism.[14] These studies confirm that reactants that prefer s-(E) conformations tend to undergo stepwise reaction. The degree of scrambling is also affected by carbene stability, migratory abilities, and nucleophilicity of solvent. The observation that the migratory ability of a substituent is inversely proportional to amount of carbene formed, indicates that under photolysis, there are competing pathways for many Wolff reactions.[14] The only Wolff rearrangements that show no scrambling are s-(Z) constrained cyclic α-diazoketones.[13]

Mechanistic conclusion[edit]

Under both thermolytic and photolytic conditions, there exist competing concerted and stepwise mechanisms. Many mechanistic studies have been carried out, including conformational, sensitization, kinetic, and isotopic scrambling studies. These all point to competing mechanisms, with general trends. α-diazoketones that exist in the s-(Z) conformation generally undergo a concerted mechanism, while those in the s-(E) conformation undergo a stepwise mechanism.[1] α-diazoketones with better migratory groups prefer a concerted mechanism.[1] However, for all substrates except cyclic α-diazoketones that exist solely in the s-(Z) conformation, products come from a combination of both pathways.[1] Transition metal mediated reactions are quite varied; however, they generally prefer forming the metal carbene intermediate.[2] The complete mechanism under photolysis can be approximated in the following figure:

Mechanistic landscape of the Wolff-rearrangement, with the concerted mechanism on the top and stepwise mechanism with carbene and oxirene intermediates on the bottom.

Migratory trends[edit]

The mechanism of the Wolff rearrangement is dependent on the aptitude of the migratory group. Migratory abilities have been determined by competition studies. In general, hydrogen migrates the fastest, and alkyl and aryl groups migrate at approximately the same rate, with alkyl migrations favored under photolysis, and aryl migrations preferred under thermolysis.[15] Substituent effects on aryl groups are negligible, with the exception of NO2, which is a poor migrator.[15] In competition studies, electron deficient alkyl, aryl, and carbonyl groups cannot compete with other migrating groups, but are still competent.[16][17][18] Heteroatoms, in general, are poor migratory groups, because their ability to donate electron density from their p orbitals into the π* C=O bond decreases migratory ability.[1] The trend is as follows:[1]

Photochemical reactions: H > alkyl ≥ aryl >> SR > OR ≥ NR2

Thermal reactions H > aryl ≥ alkyl (heteroatoms do not migrate)

Preparation of α-diazocarbonyl compounds[edit]

While known since 1902, the Wolff rearrangement did not become synthetically useful until the early 1930s, when efficient methods became available to synthesize α-diazocarbonyl compounds. The primary ways to prepare these substrates today are via the Arndt-Eistert procedure, the Franzen modification to the Dakin-West reaction, and diazo-transfer methods.

Arndt-Eistert procedure[edit]

The Arndt-Eistert Procedure[19] involves the acylation of diazomethane with an acid chloride, to yield a primary α-diazoketone. The carbon terminus of diazomethane adds to the carbonyl, to create a tetrahedral intermediate, which eliminates chloride. The chloride then deprotonates the intermediate to give the α-diazoketone product.

Part 1 of Arndt-Eistert procedure

These α-diazoketones are unstable under acidic conditions, as the α-carbon can be protonated by HCl and SN2 displacement of nitrogen can occur by chloride.

Part 2 of Arndt-Eistert procedure

Thus, triethylamine or a second equivalent of diazomethane must be added to scavenge the HCl produced in order to prevent decomposition.[20]

Part 3 of Arndt-Eistert procedure

This reaction is occasionally done with acid anhydrides, which yields a one-to-one mixture of α-diazoketone and the corresponding methyl ester.[21] This method can also be used with primary diazoalkanes, to produce secondary α-diazoketones. However, there are many limitations. Primary diazoalkanes undergo azo coupling to form azines; thus the reaction conditions must be altered such that acid chloride is added to a solution of diazoalkane and triethylamine at low temperature.[22][23] In addition, primary diazoalkanes are very reactive, incompatible with acidic functionalities, and will react with activated alkenes including unsaturated carbonyls to give 1,3-dipolar cycloaddition products.

Franzen modification to Dakin-West reaction[edit]

The Dakin–West reaction is a reaction of an amino acid with an acid anhydride in the presence of a base to form keto-amides. The Franzen modification[22] to the Dakin–West reaction[24] is a more effective way to make secondary α-diazoketones. The Franzen modification nitrosates the keto-amide with N2O3 in acetic acid, and the resulting product reacts with methoxide in methanol to give the secondary α-diazoketone.

Franzen modification to Dakin-West reaction

Diazo-transfer reactions[edit]

Diazo-transfer reactions are commonly used methods, in which an organic azide, usually tosylazide, and an activated methylene (i.e. a methylene with two withdrawing groups) react in the presence of a base to give an α-diazo-1,3-diketone.[25] The base deprotonates the methylene, yielding an enolate, which reacts with tosylazide and subsequently decomposes in the presence of a weak acid, to give the α-diazo-1,3-diketone.


The necessary requirement of two electron withdrawing groups makes this reaction one of limited scope. The scope can be broadened to substrates containing one electron withdrawing group by formylating a ketone via a Claisen condensation, followed by diazo-transfer and deformylative group transfer.[26]

Formylative diazo-transfer

One of the greatest advantages of this method is its compatibility with unsaturated ketones. However, to achieve kinetic regioselectivity in enolate formation and greater compatibility with unsaturated carbonyls, one can induce enolate formation with lithium hexamethyldisilazide and subsequently trifluoroacylate rather than formylate.[27]

Danheiser diazo-transfer

Methods for inducing rearrangement[edit]

Wolff rearrangements can be induced under thermolytic,[3] photolytic,[4] and transition-metal-catalyzed conditions.[3]

Thermal conditions to induce rearrangement require heating to relatively high temperatures, of 180 ˚C, and thus have limited use.[3] Many Wolff rearrangement products are ring-strained and are susceptible to ring-open under high temperatures. In addition, SN2 substitution of the diazo group at the α-carbon can take place at lower temperatures than rearrangement, which results in byproducts. The greatest use of thermal Wolff rearrangements is the formation of carboxylic acid analogs, by interception of the ketene with high boiling solvents, such as aniline and phenol.[3]

Transition metals greatly lower the temperature of Wolff rearrangements, by stabilization of a metal-carbene intermediate. However, these carbenes can be so stable, as to not undergo rearrangement. Carbenes of rhodium, copper, and palladium are too stable and give non-Wolff products (primarily carbene insertion products).[2] The most commonly used metal catalyst is silver(I) oxide, although silver benzoate is also common. These reactions are generally run in the presence of a weak base, such as sodium carbonate or tertiary amines.[2]

While thermal and metal mediated Wolff rearrangements date back to 1902,[3] photolytic methods are somewhat newer, with the first example of a photolytic Wolff rearrangement reported in 1951.[4] α-diazoketones have two absorption bands, an allowed π→π* transition at 240–270 nm, and a formally forbidden π→σ* transition at 270–310 nm.[4] Medium or low-pressure mercury arc lamps can excite these respective transitions. Triplet sensitizers result in non-Wolff carbene byproducts, and thus are not useful in synthetic applications of the Wolff rearrangement.[2] However, they have been used to probe the mechanism of the Wolff rearrangement.

Synthetic uses[edit]

The Wolff rearrangement has a few retrons, depending on the reaction out of the ketene intermediate. A carboxylic acid derivative with an α-methylene group is a retron for an Arndt-Eistert type homologation. An acid in which the α-carbon belongs to a ring is a retron for a Wolff rearrangement ring contraction.

Wolff Retrons

Homologation reactions[edit]

In the Arndt-Eistert homologation reaction, a carboxylic acid and thionyl chloride are reacted to generate an acid chloride. The acid chloride then reacts with diazomethane (R2 = H), or occasionally a diazoalkyl, via the Arndt-Eistert procedure, to generate an α-diazoketone, which will undergo a metal-catalyzed or photolyzed Wolff rearrangement, to give a ketene. The ketene can be trapped with any weak acid, such as an alcohol or amine, to form the ester or amide. However, trapping with water, to form the acid is the most common form.

General homologation reaction, Arndt-Eistert has R2 = H, RXH=H2O

In the most basic form, where R2= H, RXH=H2O, the reaction lengthens the alkyl chain of a carboxylic acid by a methylene. However, there is great synthetic utility in the variety of reactions one can carry out, by varying the diazoalkyl and weak acid. The migrating group, R1 migrates with complete retention.[2] A very useful application of the Arndt-Eistert homologation forms the homologated aldehyde by either trapping the ketene with N-methyl aniline and reducing with lithium aluminum hydride, or trapping the ketene with ethanethiol and reducing with Raney nickel.[28][29]

Reductive methods to make homologated aldehydes.

There exist many hundreds of examples of the Arndt-Eistert homologation in the literature.[30] Prominent examples in natural product total synthesis include the syntheses of (-)-indolizidine and (+)-macbecin.[31][32] A recent example of the Arndt-Eistert homologation is a step in the middle stage of Sarah Reisman's synthesis of (+)-salvileucalin B.[33]

Arndt-Eistert homologation in synthesis of (+)-salvileucalin B

Ring contractions[edit]

If the reactant is a cyclic α-diazoketone, then Wolff-rearrangement products will be the one-carbon ring-contracted product. These reactions are generally concerted due to the s-(Z) conformation, and are photocatalyzed. The reaction below shows the concerted mechanism for the ring contraction of α-diazocyclohexanone, followed by trapping of the ketene with a weakly acidic nucleophile.

Ring contraction of  α-diazocyclohexanone via Wolff-rearrangement

The first known example is the ring contracted Wolff rearrangement product of α-diazocamphor, and subsequent kinetic hydration of the ketene from the more sterically accessible "endo" face, to give exo-1,5,5-trimethylbicyclo[2.1.1]hexane-6-carboxylic acid.[34]

Ring contraction of α-diazocamphor via Wolff-rearrangement, followed by hydration from more sterically accessible endo face.

Ring contractions have been used extensively to build strained ring systems, as ring size does not impede the Wolff rearrangement, but often impedes other reactions. There are many examples where the Wolff rearrangement is used to contract cyclopentanone to cyclobutane.[35] The rearrangement is commonly used to form strained bicyclic and ring-fused systems. There exist a handful of examples of ring contractions from cyclobutanones to cyclopropanes.[36] The Wolff rearrangement is capable of contracting cyclohexanones to cyclopentanes, but is infrequently used to do so, because the Favorskii rearrangement accomplishes this transformation and the Wolff precursor is often more challenging to synthesize.[2] However, an example of a cyclohexanone ring contraction using deformylative diazo transfer, followed by a Wolff rearrangement, is Keiichiro Fukumoto's synthesis of (±)-∆9(12)-capnellene.[37]

Application of Wolff rearrangement ring-contraction in the Fukumoto synthesis of capnellene

Cycloaddition reactions[edit]

Ketene intermediates produced via the Wolff rearrangement are well known to undergo [2 + 2] thermal cycloadditions with olefins to form four-membered rings in both intermolecular and intramolecular reactions, examples of both are shown below.[38][39][40] Ketenes are able to undergo what is normally considered a forbidden [2 + 2] cycloaddition reaction because the ketene acts in an antarrafactial manner, leading to the Woodward-Hoffmann allowed [πs2 + πa2] cycloaddition.[39] Ketene [2 + 2] cycloadditions can be difficult reactions and give poor yields due to competing processes. The high energy aldoketene is very reactive and will cyclize with the diazoketone starting material to produce butenolides and pyrazoles.[2]

Intermolecular and intramolecular ketene [2+2] cycloadditions

Ketene [2 + 2] cycloaddition reactions have been used in many total syntheses since Corey's use of the [2 + 2] cyclization in synthesizing the prostaglandins.[38] Robert Ireland's synthesis of (±)-aphidicolin uses the Wolff rearrangement to do a tandem ring-contraction, and [2 + 2] cycloaddition.[41]

Synthesis of (±)-aphidicolin

The Danheiser benzannulation photolyses α-diazoketones and traps with an alkyne, which undergoes a pericyclic cascade, to ultimately form versatilely substituted phenols.[42] The first step in the benzannulation is the photolysis of an α-diazoketone to form a vinylketene. The vinylketene then undergoes a [2 + 2] cycloaddition with an alkyne to form a 2-vinylcyclobutenone, which does a 4π electrocyclic ring-opening to generate a dienylketene. The dienylketene subsequently undergoes a 6π electrocyclic ring-closure followed by tautomerization, to form the phenolic benzannulated product.

Danheiser Benzannulation

Vinylogous Wolff rearrangements[edit]

The vinylogous Wolff rearrangement consists of a β,γ-unsaturated diazoketone undergoing a Wolff rearrangement, and a formal 1,3-shift of the CH2CO2R group. The vinylogous Wolff rearrangement yields a γ,δ-unsaturated carboxylic acid derivative, which is the same retron as for the Claisen rearrangement. The variant was discovered when it was noticed that thermolysis of 1-diazo-3,3,3-triarylpropan-2-ones gave unexpected isomeric products.[43]

First example of vinylogous Wolff rearrangement.

Copper (II) and rhodium (II) salts tend to give vinylogous Wolff rearranged products, and CuSO4 and Rh2(OAc)4 are the most commonly used catalysts.[44] This is because they promote metal carbene formation, which can add to the olefin to form a cyclopropane, which can reopen via a retro [2 + 2] to form a formally 1,3-shifted ketene (vis-à-vis a normal Wolff rearranged ketene), which can be trapped by a nucleophile to give the vinylogous Wolff product.[45]

Mechanism for vinylogous Wolff rearrangement.

See also[edit]


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