Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433936Generated: October 25, 2026

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

https://huagongshe.com/reaction/433936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetyl chlorideHCID 6577—
Reactant1,3-DifluorobenzeneHCID 9741—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloro-1-(2,4-difluorophenyl)ethanoneHCID 58808375%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into the solution of 1,3-difluorobenzene in 1,2-dicholoroethane (DCE) was added anhydrous aluminium chloride (1.2 molar equivalent of 1,3-difluorobenzene) at 25-30° C. and stirred for 30 minutes. The reaction mixture was then cooled to 0° C. and chloroacetyl chloride (1.1 molar equivalent of 1,3-difluorobenzene), in DCE, was then added into it over a period of 30-60 min keeping the reaction temperature below 20° C. After the addition was over, the reaction mixture was stirred at 25-30° C. for 5-7 hours. The reaction mixture was then diluted with DCE and poured into dil. hydrochloric acid (5%) at 0-5° C. The mixture was then extracted with DCE. The combined organic layer was washed successively with 5% aq. sodium bicarbonate solution and water. Evaporating DCE from the organic layer under reduced pressure gave an oil which on triturating with n-Hexane gave the title compound as white crystalline material (Yield 75% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670363B1
Source datasetuspto-grants-2003_12
ORD IDord-186f0a5f3da4434294b577da0c0bf1d7
Source noteuspto-grants-2003_12