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Lawesson's reagent

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Lawesson's reagent
Lawesson's reagent
3D model of the Lawesson's reagent molecule
Names
IUPAC name
2,4-Bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide
Preferred IUPAC name
2,4-Bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-dithione
Other names
Lawesson reagent; LR
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.038.944 Edit this at Wikidata
  • InChI=1S/C14H14O2P2S4/c1-15-11-3-7-13(8-4-11)17(19)21-18(20,22-17)14-9-5-12(16-2)6-10-14/h3-10H,1-2H3 checkY
    Key: CFHGBZLNZZVTAY-UHFFFAOYSA-N checkY
  • InChI=1/C14H14O2P2S4/c1-15-11-3-7-13(8-4-11)17(19)21-18(20,22-17)14-9-5-12(16-2)6-10-14/h3-10H,1-2H3
    Key: CFHGBZLNZZVTAY-UHFFFAOYAB
  • S=P1(SP(=S)(S1)c2ccc(OC)cc2)c3ccc(OC)cc3
Properties
C14H14O2P2S4
Molar mass 404.45 g·mol−1
Appearance Slightly yellow powder
Melting point 228–231 °C (442–448 °F; 501–504 K)
Insoluble
Related compounds
Related thiation agents
Hydrogen sulfide,
Phosphorus pentasulfide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Lawesson's reagent, or LR, is a chemical compound used in organic synthesis as a thiation agent. Lawesson's reagent was first made popular by Sven-Olov Lawesson, who did not, however, invent it. Lawesson's reagent was first made in 1956 during a systematic study of the reactions of arenes with P4S10.[1]

Preparation

Lawesson's reagent is commercially available. It can also be conveniently prepared in the laboratory by heating a mixture of anisole with phosphorus pentasulfide until the mixture is clear and no more hydrogen sulfide is formed,[2] then recrystallized from toluene or xylene.

As Lawesson's reagent has a strong and unpleasant smell, it is best to prepare the compound within a fume-hood and to treat all glassware used with a decontamination solution before taking the glassware outside the fume-hood. One common and effective method of destroying the foul smelling residues is to use an excess of sodium hypochlorite (chlorine bleach).

Mechanism of action

Lawesson's reagent has a four membered ring of alternating sulfur and phosphorus atoms. With heating, the central phosphorus/sulfur four-membered ring can open to form two reactive dithiophosphine ylides (R-PS2). Much of the chemistry of Lawessons's reagent is in fact the chemistry of these reactive intermediates.

In general, the more electron rich a carbonyl is, the faster the carbonyl group will be converted into the corresponding thiocarbonyl by Lawesson's reagent.

Applications

The chemistry of Lawesson's reagent and related substances has been reviewed by several groups.[3][4][5][6] The main use of Lawesson's reagent is the thionation of carbonyl compounds. For instance, Lawesson's reagent will convert a carbonyl into a thiocarbonyl.[7] Additionally, Lawesson's reagent has been used to thionate enones, esters,[8] lactones,[9] amides, lactams,[10] and quinones.

Thionation of a ketone to give a thioketone using Lawesson's reagent

In one study, reaction of maltol with LR results in a selective oxygen replacement in two positions.[11]

Maltol reaction with LR

A combination of silver perchlorate and Lawesson's reagent is able to act as an oxophilic Lewis acid with the ability to catalyze the Diels-Alder reaction of dienes with α,β-unsaturated aldehydes.

Alcohols may be converted to thiols by treatment with Lawesson's reagent.[12]

See also

References

  1. ^ Lecher, H. Z.; Greenwood, R. A.; Whitehouse, K. C.; Chao, T. H. (1956). "The Phosphonation of Aromatic Compounds with Phosphorus Pentasulfide". J. Am. Chem. Soc. 78 (19): 5018. doi:10.1021/ja01600a058.
  2. ^ Thomsen, I.; Clausen, K.; Scheibye, S.; Lawesson, S.-O. (1990). "Thiation with 2,4-Bis(4-methoxyphenyl)-1,3,2,4-Dithiadiphosphetane 2,4-disulfide: N-Methylthiopyrrolidone". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 7, p. 372.
  3. ^ Cherkasov, R. A.; Kutyrev, G. A.; Pudovik, A. N. (1985). "Tetrahedron report number 186 Organothiophosphorus reagents in organic synthesis". Tetrahedron (Review). 41 (41): 2567. doi:10.1016/S0040-4020(01)96363-X.
  4. ^ Foreman, M.S.; Woollins, J.D. (2000). "Organo-P-S and P-Se heterocycles". J. Chem. Soc., Dalton Trans. (10): 1533–1543. doi:10.1039/b000620n.
  5. ^ Martin Jesberger; Thomas P. Davis; Leonie Barner (2003). "Applications of Lawesson's Reagent in Organic and Organometallic Syntheses". Synthesis (Review). 2003 (13): 1929–1958. doi:10.1055/s-2003-41447.
  6. ^ Cava, M. P.; Levinson, M. I. (1985). "Thionation reactions of Lawesson's reagents". Tetrahedron. 41 (22): 5061–5087. doi:10.1016/S0040-4020(01)96753-5.
  7. ^ Pedersen, B. S.; Scheibye, S.; Nilsson, N. H.; Lawesson, S.-O. (1978). Bull. Soc. Chim. Belg. (87): 223. {{cite journal}}: Missing or empty |title= (help)CS1 maint: multiple names: authors list (link)
  8. ^ Jones, B. A.; Bradshaw, J. S. (1984). "Synthesis and reduction of thiocarboxylic O-esters". Chem. Rev. (Review). 84 (84): 17. doi:10.1021/cr00059a002.
  9. ^ Scheibye, S.; Kristensen, J.; Lawesson, S.-O. (1979). "Studies on organophosphorus compounds—XXVII Synthesis of thiono-, thiolo- and dithiolactones". Tetrahedron. 35 (35): 1339. doi:10.1016/0040-4020(79)85027-9.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Shabana, R.; Scheibye, S.; Clausen, K.; Olesen, S. O.; Lawesson, S.-O. (1980). Nouveau Journal de Chimie. 1980 (4): 47. {{cite journal}}: Missing or empty |title= (help)CS1 maint: multiple names: authors list (link)
  11. ^ Brayton, D.; Jacobsen, F. E.; Cohen, S. M.; Farmer, P. J. (2006). "A novel heterocyclic atom exchange reaction with Lawesson's reagent: a one-pot synthesis of dithiomaltol". Chemical Communications. 2006 (2): 206–208. doi:10.1039/b511966a. PMID 16372107.
  12. ^ Nishio, Takehiko (1989). "A novel transformation of alcohols to thiols". Journal of the Chemical Society, Chemical Communications. 1989 (4): 205–206. doi:10.1039/C39890000205.