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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713588Generated: November 1, 2026

4-Ethylbenzoyl chloride → (5-Bromo-2-chloro-4-methoxyphenyl)(4-ethylphenyl)methanone

https://huagongshe.com/reaction/1713588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethylbenzoyl chlorideHCID 85368—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Bromo-4-chloro-2-methoxybenzeneHCID 17984845—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-2-chloro-4-methoxyphenyl)(4-ethylphenyl)methanoneHCID 4620679669%

Reaction Steps

To a solution of 1-bromo-4-chloro-2-methoxybenzene (5.1 g, 23 mmol) and 4-ethylbenzoyl chloride (4.1 g, 24 mmol) in 15 mL of anhydrous dichloromethane (DCM) was added aluminum trichloride (3.2 g, 24 mmol). The mixture was stirred at room temperature for 1 hour, followed by heating at reflux for 18 hours. The mixture was poured into 100 mL of ice-cold water and the organic layer was isolated. The aqueous solution was extracted with 25 mL DCM. The combined organic extracts were washed with brine (25 mL), dried (Na2SO4), filtered, and evaporated. Recrystallization from petroleum ether gave the intermediate (5-bromo-2-chloro-4-methoxyphenyl)(4-ethylphenyl)methanone 21 (5.6 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795228B2
Source datasetuspto-grants-2010_09
ORD IDord-cd0845e4fd6648d1b4fad80496a26f96
Source noteuspto-grants-2010_09