Dibenzylideneacetone: Difference between revisions

| Verifiedfields = changed

| verifiedrevid = 426563629

| ImageFile = (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one 200.svg

| ImageFile2 = Dibenzylideneacetone Crystals.jpg

| ImageSize2 = 220px

| PIN = (1''E'',4''E'')-1,5-Diphenylpenta-1,4-dien-3-one

|Section1={{Chembox Identifiers

| ChemSpiderID = 86113

| ChemSpiderID_Comment = undefined

| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID1 = 555548

| ChemSpiderID1_Comment = (''E'',''E'')

| ChemSpiderID1_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID2 = 1266463

| ChemSpiderID2_Comment = (''E'',''Z'')

| ChemSpiderID2_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID3 = 1266462

| ChemSpiderID3_Comment = (''Z'',''Z'')

| ChemSpiderID3_Ref = {{chemspidercite|changed|chemspider}}

| InChI = 1S/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H

| InChI_Comment = undefined

| InChI1 = 1S/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H/b13-11+,14-12+

| InChI1_Comment = (''E'',''E'')

| InChI2 = 1S/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H/b13-11-,14-12+

| InChI2_Comment = (''E'',''Z'')

| InChI3 = 1S/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H/b13-11-,14-12-

| InChI3_Comment = (''Z'',''Z'')

| InChIKey = WMKGGPCROCCUDY-UHFFFAOYSA-N

| InChIKey1 = WMKGGPCROCCUDY-PHEQNACWSA-N

| InChIKey2 = WMKGGPCROCCUDY-HEEUSZRZSA-N

| InChIKey3 = WMKGGPCROCCUDY-XSYHWHKQSA-N

| SMILES = O=C(C=Cc1ccccc1)C=Cc2ccccc2

| SMILES_Comment = undefined

| SMILES1 = O=C(/C=C/c1ccccc1)/C=C/c2ccccc2

| SMILES1_Comment = (''E'',''E'')

| SMILES2 = O=C(\C=C\c1ccccc1)/C=C\c2ccccc2

| SMILES2_Comment = (''E'',''Z'')

| SMILES3 = O=C(/C=C\c1ccccc1)/C=C\c2ccccc2

| SMILES3_Comment = (''Z'',''Z'')

| CASNo_Ref = {{cascite|correct|CAS}}

| CASNo_Comment = non-specific

| CASNo1_Ref = {{cascite|correct|CAS}}

| CASNo1 = 35225-79-7

| CASNo1_Comment = (''E'',''E'')

| CASNo2_Ref = {{cascite|correct|CAS}}

| CASNo2 = 115587-57-0

| CASNo2_Comment = (''E'',''Z'')

| CASNo3_Ref = {{cascite|correct|CAS}}

| CASNo3 = 58321-78-1

| CASNo3_Comment = (''Z'',''Z'')

| PubChem = 95417

| PubChem_Comment = undefined

| PubChem1 = 640180

| PubChem1_Comment = (''E'',''E'')

| PubChem2 = 1549622

| PubChem2_Comment = (''E'',''Z'')

| PubChem3 = 1549621

| PubChem3_Comment = (''Z'',''Z'')

| ChEMBL1_Ref = {{ebicite|changed|EBI}}

| ChEMBL1 = 17201

| ChEMBL1_Comment = (''E'',''E'')

| UNII1_Ref = {{fdacite|correct|FDA}}

| UNII1 = 9QXO7BCY9L

| UNII1_Comment = (''E'',''E'')

| UNII2_Ref = {{fdacite|correct|FDA}}

| UNII2 = N4SH2VDI6Y

| UNII2_Comment = (''E'',''Z'')

| UNII3_Ref = {{fdacite|correct|FDA}}

| UNII3 = 5L4OCE3E5U

| UNII3_Comment = (''Z'',''Z'')

|Section2={{Chembox Properties

| MeltingPt_notes = {{ubli

| {{convert|110-111|°C|°F K}} (''trans'', ''trans'' isomer)<ref name=OrgSynth/>

| {{convert|60|°C|°F K}} (''cis'', ''trans'' isomer)<ref name=Merck>Merck index</ref>

| BoilingPtC = 130

| BoilingPt_notes = (''cis'', ''cis'' isomer)<ref name=Merck/>

| Solubility = Insoluble

| Solvent = other solvents

| SolubleOther = Soluble in acetone and chloroform, slightly soluble in ethanol.

}}

|Section3={{Chembox Hazards

| AutoignitionPt =

'''Dibenzylideneacetone''' or '''dibenzalacetone''', often abbreviated '''dba''', is an [[organic compound]] with the formula C₁₇H₁₄O. It is a pale-yellow solid insoluble in water, but soluble in ethanol.

It was first prepared in 1881 by the German chemist [[Rainer Ludwig Claisen]] (1851–1930) and the Swiss chemist Charles-Claude-Alexandre Claparède (14 April 1858 – 1 November 1913).<ref>{{cite journal|last1=Claisen|first1=L.|last2=Claparède|first2=A.|title=Ueber Verbindungen des Acetons und Mesityloxds mit Benzaldehyd und über die Constitution des Acetophorons|journal=Berichte der Deutschen Chemischen Gesellschaft|date=1881|volume=14|pages=349–353|url=https://babel.hathitrust.org/cgi/pt?id=hvd.cl1hza;view=1up;seq=421|trans-title=On compounds of acetone and [[mesityl oxide]] with benzaldehyde and on the composition of [[phorone]]|language=German|doi=10.1002/cber.18810140182}} ; see pp. 350–351.</ref><ref>Claisen wrote that the German chemist [[Adolf von Baeyer|Adolf Baeyer]] might have synthesized dibenzylideneacetone as early as 1866, although the evidence wasn't clear.

* (Claisen & Claparède, 1881), p. 350: ''"Die Einwirkung wasserentziehender Mittel auf ein solches Gemenge ist schon von Baeyer¹) flüchtig untersucht worden. Nach ihm entsteht als Endprodukt ein gelbes, in Alkohol unlösliches Harz, als Zwischenprodukt ein ölförmiger, unzersetzt siedender und cumarinartig riechender Körper, der, wie er meint, das Methylketon der Zimmtsäure darstellt."'' (The effect of a dehydrating agent on such a mixture has already been briefly investigated by Baeyer¹). According to him, a yellow resin [that's] insoluble in alcohol arises as a final product, [and] as an intermediate, [there arises] an oily substance [which] boils without decomposing and smells like coumarin [and] which, he thinks, represents the methyl ketone of cinnamic acid.)

* {{cite journal|last1=Baeyer|first1=Adolf|title=Ueber Condensation und Polymerie|journal=Annalen der Chemie und Pharmacie |date=1866|volume=5|issue=Supplement|pages=79–95|url=https://babel.hathitrust.org/cgi/pt?id=iau.31858002361610;view=1up;seq=87|trans-title=On condensation and polymerism|language=German}} ; see p. 82. From p. 82: ''"Um für diese Ansicht noch einen weiteren Beweis beizubringen, habe ich ein Gemenge von Bittermandelöl und Aceton mit wasserentziehenden Mitteln, Salzsäure, Schwefelsäure, Kali behandelt. Die Condensation erfolgt ausserordentlich schnell, schon nach wenigen Minuten, und nach einiger Zeit verharzt die ganze Masse. Das Endproduct ist ein gelbes Harz, das in Aether löslich und durch Alkohol daraus als gelbes Pulver gefällt wird, welches schwach nach Rhabarber riecht. Die Analyse gab keine verständlichen Zahlen, daher ist die Substanz wahrscheinlich ein Gemenge. Zuerst bildet sich aber ein öliger, unzersetzt flüchtiger Körper, der einen an Cumarin erinnernden Geruch besitzt, und der höchst wahrscheinlich das Methylaceton der Zimmtsäure ist: … ."'' (In order to provide further proof for this view, I have treated a mixture of benzaldehyde and acetone with dehydrating agents [e.g.,] hydrochloric acid, sulfuric acid, potash. The condensation occurs extraordinarily quickly, after just a few minutes, and after some time the whole mass becomes resinous. The final product is a yellow resin, which [is] soluble in ether and is precipitated therefrom by alcohol as a yellow powder, which smells faintly of rhubarb. Analysis [to determine its empirical formula] produced no intelligible numbers, so the substance is probably a mixture. Initially, however, an oily, stable, volatile substance is formed, which has a smell recalling coumarin, and which is very likely the methyl acetone of cinnamic acid: … .)</ref><ref>For biographical information about Charles-Claude-Alexandre Claparède (with photograph), see: Reverdin, Frédéric (1914) [https://babel.hathitrust.org/cgi/pt?id=mdp.39015035501173;view=1up;seq=892 "Dr. Alexandre Claparède. 1858–1913,"] ''Verhandlungen der Schweizerischen Naturforschenden Gesellschaft: Nekrologe und Biographien verstorbener Mitglieder'' … (Proceedings of the Swiss Society of Natural Sciences: Obituaries and biographies of deceased members … ), '''96''' : 22–27. (in French)</ref>

==Preparation==

{{main|Claisen-Schmidt condensation}}

The ''trans'',''trans'' isomer can be prepared in high yield and purity by [[Aldol condensation|condensation]] of [[benzaldehyde]] and [[acetone]] with [[sodium hydroxide]] in a water/ethanol medium followed by [[recrystallization (chemistry)|recrystallization]].<ref name=OrgSynth>{{OrgSynth |author1=Conard, C. R.|author2=Dolliver, M. A. | title = Dibenzalacetone | collvol = 2 | collvolpages = 167 | year = 1943 | prep=cv2p0167}}</ref>

:[[Image:Synthesis Dibenzylideneaceton.svg|500px|Dibenzalacetone synthesis]]

This reaction, which proceeds via the intermediacy of [[benzylideneacetone]], is often performed in [[organic chemistry]] classes,<ref>{{cite journal | title=The Dibenzalacetone Reaction Revisited | author1=Hull, L. A. | date=February 2001 | journal=[[Journal of Chemical Education|J. Chem. Educ.]] | volume=78 | issue=2 | pages=226 | doi=10.1021/ed078p226 | bibcode=2001JChEd..78..226H | url=https://pubs.acs.org/doi/abs/10.1021/ed078p226}}</ref> and is called [[Claisen-Schmidt condensation]].

==Reactions and derivatives==

Prolonged exposure to sunlight initiates [2+2] [[cycloaddition]]s, converting it to a mixture of dimeric and trimeric [[cyclobutane]] [[adduct|cycloadduct]]s.<ref>{{cite journal | title=Photochemical Dimerization of Dibenzylideneacetone. A Convenient Exercise in <nowiki>[2+2]</nowiki> Cycloaddition Using Chemical Ionization Mass Spectrometry |author1=Rao, G. N. |author2=Janardhana, C. |author3=Ramanathan, V. |author4=Rajesh, T. |author5=Kumar, P. H. |date=November 2006 | journal=[[Journal of Chemical Education|J. Chem. Educ.]] | volume=83 | issue=11 | pages=1667 | url=http://jchemed.chem.wisc.edu/Journal/issues/2006/Nov/abs1667.html | doi=10.1021/ed083p1667|bibcode=2006JChEd..83.1667R }}</ref>

==Uses==

Dibenzylideneacetone is used as a component in [[sunscreen]]s and as a [[ligand]] in [[organometallic chemistry]].

For example, it is a component of the catalyst [[tris(dibenzylideneacetone)dipalladium(0)]]. It is a labile ligand that is easily displaced by [[triphenylphosphine]], hence it serves a useful entry point into [[palladium]](0) chemistry.

[[Category:Enones]]