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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436382Generated: October 30, 2026

(4-Chlorophenyl)acetic acid → Ethanone, 2-(4-chlorophenyl)-1-phenyl-

https://huagongshe.com/reaction/436382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
ReactantThionyl ChlorideHCID 24386—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
ProductEthanone, 2-(4-chlorophenyl)-1-phenyl-HCID 95829142.4%

Reaction Steps

A benzene solution containing 51.2 g 4-chlorophenylacetic acid and 39.3 g thionyl chloride is refluxed for 6 hours and the solvent removed. The crude reaction product is added dropwise to a slurry of 40 g aluminum chloride in 200 ml benzene maintaining the temperature below 50° C. After addition the reaction is refluxed for 1.5 hours. After cooling, the mixture is poured into ice and the resulting white solid is separated yielding 61.3 g of crude product. The product is taken up in methylene chloride and washed with 5% sodium hydroxide solution followed by water, dried over sodium sulfate and stripped yielding 49.3 g (71%) of >95% pure 4'-chlorodeoxybenzoin. 15 g of 4-chlorodeoxybenzoin is dissolved in 105 ml pyridine. An aqueous solution containing 15 g potassium permanganate is added and the reaction stirred for 6 hours at room temperature using dry ice to buffer the pH near 7. The mixture is extracted with methylene chloride, the extract washed with water, dried over Na2SO4 and stripped. The residue is recrystallized from ethanol yielding 6.1 g of white plate-like crystals which is identified as starting material. Concentration of the mother liquor yields 4 g of 4-chlorobenzil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009022
Source datasetuspto-grants-1977_02
ORD IDord-b51ce1ad36624850985a193b27954a53
Source noteuspto-grants-1977_02