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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263584Generated: November 2, 2026

Dimethylformamide → (5-Bromo-2-chloro-phenyl)-(4-ethoxy-phenyl)-methanone

https://huagongshe.com/reaction/2263584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
ReactantOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-2-chloro-phenyl)-(4-ethoxy-phenyl)-methanoneHCID 22328608—

Reaction Conditions

Temperature-5 °C

Reaction Steps

38.3 ml oxalyl chloride and 0.8 ml of dimethylformamide are added to a mixture of 100 g of 5-bromo-2-chloro-benzoic acid in 500 ml dichloromethane. The reaction mixture is stirred for 14 h, then filtered and separated from all volatile constituents in rotary evaporator. The residue is dissolved in 150 ml dichloromethane, the solution is cooled to −5° C., and 46.5 g of anisole are added. Then 51.5 g of aluminium trichloride are added batchwise so that the temperature does not exceed 5° C. The solution is stirred for another 1 h at 1-5° C. and then poured onto ice. The organic phase is separated off and the aqueous phase is extracted another three times with dichloromethane. The combined organic phases are washed with aqueous 1 M hydrochloric acid, twice with 1 M sodium hydroxide solution and with saturated sodium chloride solution. Then the organic phase is dried, the solvent is removed and the residue is recrystallised from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851602B2
Source datasetuspto-grants-2010_12
ORD IDord-def4600d437c462f8ff229b93359dbfe
Source noteuspto-grants-2010_12