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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510818Generated: October 31, 2026

1-(3-Bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone → 3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrile

https://huagongshe.com/reaction/510818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanoneHCID 12027479—
ReactantHCID 178418260HCID 178418260—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrileHCID 5836851698.1%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 1-(3-bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone (4.9 g, 18 mmol) and copper cyanide (2.5 g, 28 mmol) in N-methylpyrrolidinone (15 mL) was heated at 200° C. for 1 hour. The resulting mixture was allowed to cool to room temperature and was then diluted with ethyl acetate and 1 N HCl. The organic and aqueous layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over magnesium sulfate and concentrated to dryness under reduced pressure to give 3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrile (3.7 g, 96%). LCMS calculated for C10H9ClNO2 (M+H)+: m/z=210.0. found: 210.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-e26a8688d3334d7a81ce667f61f1c037
Source noteuspto-grants-2015_08