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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732629Generated: November 1, 2026

Benzoyl chloride → (4-Cyclohexylphenyl)(phenyl)methanone

https://huagongshe.com/reaction/1732629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCyclohexylbenzeneHCID 13229—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product(4-Cyclohexylphenyl)(phenyl)methanoneHCID 26588075%

Reaction Steps

67 g (0.5 mol) of aluminium chloride are added in portions to a mixture of 80 g (0.5 mol) of cyclohexylbenzene 70 g (0.5 mol) of benzoyl chloride and 500 ml of methylene chloride at room temperature. After 15 hours, the reaction mixture is poured onto ice/hydrochloric acid. The organic phase is washed with water until neutral, dried over sodium sulphate and evaporated. The crude product is purified by distillation. 93.3 g (75% of theory) of 4-cyclohexylbenzophenone of boiling point 160° to 175° C./0.1 mm are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238498
Source datasetuspto-grants-1980_12
ORD IDord-8f91a212420449fbb3fffc75dd7d4e02
Source noteuspto-grants-1980_12