Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041853Generated: October 31, 2026

Acetyl chloride → Methyl 3-cyano-4-fluorobenzoate

https://huagongshe.com/reaction/1041853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Cyano-4-fluorobenzoic acidHCID 2773932—
SolventMethanolHCID 887—
ProductMethyl 3-cyano-4-fluorobenzoateHCID 4579012378.1%

Reaction Steps

To a stirred suspension of 16.0 g (96.9 mmol) 2a and 161 ml methanol were added 30.4 g (387.6 mmol) acetyl chloride drop wisely at 0° C. The reaction mixture was stirred over night, filtered and concentrated. The residue was diluted with dichloromethane, washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The residue was purified by column chromatography (hexane:ethylacetate). The desired product 2b was obtained in 78.1% yield (13.5 g; 75.7 mmol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557776B2
Source datasetuspto-grants-2013_10
ORD IDord-a6186fa964304221bdaa232d03d2a949
Source noteuspto-grants-2013_10