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Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → (E)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl ester

HRID 2232757
Notes
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Reaction equation

HRID 2232757 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=2)=[CH:9][CH:10]=O)[CH:5]=[CH:6][CH:7]=1.[C:19]([CH:24]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:21][CH2:22][CH3:23])=[O:20]>C(O)C>[CH2:22]([O:21][C:19](=[O:20])/[CH:24]=[CH:10]\[CH:9]=[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=1)[C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=1)[CH3:23].[CH2:22]([O:21][C:19](=[O:20])/[CH:24]=[CH:10]/[CH:9]=[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=1)[C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=1)[CH3:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 145472273,3-Bis(3-chlorophenyl)-2-propenal

Product 2

HCID 14347255(E)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl esterHCID 86742568(Z)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl ester

Reagents, catalysts & solvents 1

HCID 702
Ethanol
Solvent

Procedure

In the manner described in Example 99, 3,3-bis(3-chlorophenyl)-2-propenal (14.6 g) was reacted with (carbethoxymethylene)triphenylphosphorane (19.15 g) in ethanol (50 ml) for 30 minutes at ambient temperature. The mixture of esters obtained from the usual work up was purified by HPLC (dichloromethanehexane; 1:2) to provide 3.2 g of the less polar (Z)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl ester as an oil, and 11.2 g of (E)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl ester. A portion of the (E)-isomer (E)-5,5-bis(3-chlorophenyl)-2,4-pentadienoic acid ethyl ester was crystallized from 2-propanol to give the ester, mp 68°-69° C.

Workup

  1. customobtained from the usual work
  2. customup was purified by HPLC (dichloromethanehexane; 1:2)

Sources & evidence

ORD record
ord-8e496af0f9bd4c69a0784902008c90b4
Source dataset
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04788206

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes