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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764612Generated: November 1, 2026

Phenylacetic Acid → HCID 343978, compound

https://huagongshe.com/reaction/1764612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantAcetic AnhydrideHCID 7918—
SolventTriethylamineHCID 8471—
ProductHCID 343978HCID 343978—

Reaction Steps

A mixture of 56.2 g 4-chlorobenzaldehyde, 54.4 g phenylacetic acid, 80 ml acetic anhydride and 40 ml triethylamine was refluxed for 5 hours. Unreacted 4-chlorobenzaldehyde was removed by steam distillation and the residue dissolved in aqueous alcohol and treated with decolourising carbon. Crystals of α-phenyl-4-chlorocinnamic acid were obtained on acidification of the solution. The product was recrystallised from alcohol and found to have a melting point of 202°-4° C. The chlorosulphonyl derivative was prepared according to the method described in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04117039
Source datasetuspto-grants-1978_09
ORD IDord-7fa6319256d24fff9e1a50e76cf3fc3f
Source noteuspto-grants-1978_09