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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189485Generated: October 30, 2026

2-(4-Fluorophenyl)acetic acid → 4-Fluorophenylacetyl chloride

https://huagongshe.com/reaction/2189485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
ReactantThionyl ChlorideHCID 24386—
Product4-Fluorophenylacetyl chlorideHCID 3744988—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Fluorophenylacetic acid [starting compound B] (15 g) was dissolved in thionyl chloride (15 ml) to prepare a solution which was then heated at 60° C. for one hr. Excess thionyl chloride was removed by evaporation under the reduced pressure to give 4-fluorophenylacetyl chloride. The acid chloride was dissolved in acetone (200 ml). Ammonium acetate (112 g) was added to the solution, and the mixture was stirred at room temperature for 17 hr. An aqueous saturated sodium hydrogencarbonate solution (150 ml) was added thereto, and the mixture was stirred at room temperature for one hr. The reaction solution was then extracted with chloroform, and the solvent in the extract was removed by evaporation to give a crude crystal. The resultant crude crystal was washed with a hexane/ethyl acetate (2/1) mixed solution to give 4-fluorophenylacetamide (10.5 g, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324245B2
Source datasetuspto-grants-2012_12
ORD IDord-18db56efe19b4f50a20cac4a3d02367f
Source noteuspto-grants-2012_12