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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276517Generated: November 2, 2026

Benzoyl chloride → 3,4-Diethylbenzophenone

https://huagongshe.com/reaction/1276517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1,2-DiethylbenzeneHCID 8657—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product3,4-DiethylbenzophenoneHCID 21584598—

Reaction Steps

A mixture of benzoyl chloride (1 eq) and 3,4-diethylbenzene (1.15 eq) was dissolved in 1,2-dichloroethane in a dry flask under argon and cooled in an ice bath with stirring. Aluminum chloride (1.3 eq) was added in portions to the reaction mixture at a rate to maintain the temperature below 10° C. Upon complete addition of the aluminum chloride, the ice bath was removed and the reaction mixture was stirred at room temperature for 18 h, then poured into cold water (100 mL) and extracted into ether (2×100 mL). The combined ether extracts were washed with water (25 mL), sodium bicarbonate solution (2×25 mL), water (25 mL), brine (25 mL), dried (MgSO4) and concentrated to provide the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166072
Source datasetuspto-grants-2000_12
ORD IDord-13992d8f48cb4fa5bed6e53ec46dbee0
Source noteuspto-grants-2000_12