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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703580Generated: October 30, 2026

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

https://huagongshe.com/reaction/1703580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantButylbenzeneHCID 7705—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product(4-Butylphenyl)(phenyl)methanoneHCID 1414873596.8%

Reaction Steps

A 2.8 g (0.02 mole) of benzoic acid chloride was dissolved in 30 ml of carbon disulfide and then, 4.0 g (0.03 mole) of anhydrous aluminum chloride was added to the solution. A 2.68 g (0.02 mole) of n-butyl benzene was further added to the mixture with stirring, and the reaction was carried out at room temperature for 18 hours. Carbon disulfide was distilled off from the reaction mixture and water was added and the reaction product was extracted with benzene. The benzene phase was separated and washed with 1N-NaOH and with water and was dried with anhydrous sodium sulfate. The solvent was distilled off to obtain a pale yellow oily product. The oily product was distilled under a reduced pressure to obtain 4.6 g of 4-n-butyl benzophenone having a boiling point of 184° to 188° C./6 mmHg. (yield of 96.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124726
Source datasetuspto-grants-1978_11
ORD IDord-ae7dc010e42c41988dc9d88c23ae4f11
Source noteuspto-grants-1978_11