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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514239Generated: October 28, 2026

Methanol → alpha-Acetyl-2-bromo-4-fluorobenzeneacetonitrile

https://huagongshe.com/reaction/514239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTolueneHCID 1140—
Reactant2-(2-Bromo-4-fluorophenyl)acetonitrileHCID 826392—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productalpha-Acetyl-2-bromo-4-fluorobenzeneacetonitrileHCID 66608202—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of sodium methoxide in methanol (25%, 34 mL, 157 mmol) was combined with toluene (200 mL). The methanol was then distilled off at 90° C. using a Dean-Stark trap. After the solution was cooled to 70° C., 2-bromo-4-fluorobenzeneacetonitrile (21.4 g, 100 mmol) dissolved in ethyl acetate (40 mL) was added from a dropping funnel over 20 min with mechanical stirring. At this point additional toluene (150 mL) was added to facilitate stirring of a voluminous light pink precipitate. The reaction mixture was poured into water, and the organic phase was separated. The aqueous phase was acidified and extracted with ethyl acetate. The ethyl acetate phase was dried and concentrated under reduced pressure to provide the intermediate compound α-acetyl-2-bromo-4-fluorobenzeneacetonitrile as a crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107412B2
Source datasetuspto-grants-2015_08
ORD IDord-0a04fffe5e1449f6864c7bacc3a19a61
Source noteuspto-grants-2015_08