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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962838Generated: October 30, 2026

Acetyl chloride → 1-(3-Fluoro-4-methoxyphenyl)ethan-1-one

https://huagongshe.com/reaction/962838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-FluoroanisoleHCID 67576—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChloroformHCID 6212—
Product1-(3-Fluoro-4-methoxyphenyl)ethan-1-oneHCID 96828—

Reaction Steps

Aluminum chloride (80.0 g, 0.6 mol) and chloroform (750 mL) were placed in a 2 L three-necked round bottom flask fitted with a mechanical stirrer and cooled by means of an ice bath. To the stirred solution was added acetyl chloride (51.0 g, 0.65 mol) dropwise, maintaining the temperature between 5°-10° C. The mixture was allowed to stir for 10 minutes at 5° C. before the dropwise addition at 5°-10° C. of 2-fluoroanisole (63.06 g, 0.5 mol. The mixture was stirred at 0°-10° C. for 1 hour and poured into ice (1 L). The resultant layers were separated and the aqueous layer was extracted with methylene chloride (2×250 mL). The combined organic layers were washed with water (2×150 mL), dried over magnesium sulfate, and concentrated to 300 mL. Hexanes crystallized from the mixture: mp 92°-94° C.; 1H NMR (d6 -DMSO) 7.8 (m, 2H), 7.3 (t, J=8.7Hz, 1H), 3.9 (s, 3H), 2.5 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760068
Source datasetuspto-grants-1998_06
ORD IDord-9e4ff675f7d5409d96f062fc9845f864
Source noteuspto-grants-1998_06