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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589821Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-1-(3,4-difluorophenyl)ethanone

https://huagongshe.com/reaction/589821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetyl chlorideHCID 6577—
Reactant1,2-DifluorobenzeneHCID 9706—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-1-(3,4-difluorophenyl)ethanoneHCID 239232170%

Reaction Conditions

Temperature60 °C

Reaction Steps

1,2-Difluorobenzene (150 g) and aluminium chloride (156 g) were charged in a round bottom flask. The reaction mixture is heated to about 60° C. followed by slow addition of chloroacetyl chloride (105 mL) over a period of 1 hour at the same temperature. The reaction mixture was stirred for another 3 hours followed by cooling to about 10° C. The reaction mass was poured into precooled water (1500 mL) followed by addition of hydrochloric acid (36%, 225 mL) at the same temperature and stirring. To this mixture ethyl acetate (750 mL) was charged and layers were separated. The aqueous layer is extracted with ethyl acetate (750 mL). The organic layers were combined and washed with water (750 mL) followed by complete evaporation of organic layer under vacuum at 50-55° C. The residue obtained is cooled to 25-35° C. followed by purification with column chromatography using 0-5% ethyl acetate in petroleum ether to afford the title compound in about 70% yield having HPLC purity of 99.51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233966B2
Source datasetuspto-grants-2016_01
ORD IDord-7d4365a7957542038a842d9eff747f40
Source noteuspto-grants-2016_01