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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192587Generated: 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/1192587

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 58368516—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 1-(3-bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone (4.85 g, 18.4 mmol) and copper cyanide (2.47 g, 27.6 mmol) in N-methylpyrrolidinone (15 mL) was heated at 200° C. for 1 hour. After cooling to room temperature, the mixture was diluted with ethyl acetate and 1 N HCl. The layers were separated and the aqeous layer was extracted with ethyl acetate. The combined organic layers were washed with water, then brine and dried over magnesium sulfate. After concentration to dryness under reduced pressure, the residue was used directly in the next step (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 numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-be56b57f80334838ad3558dd0755118b
Source noteuspto-grants-2014_03