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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499721Generated: October 30, 2026

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

https://huagongshe.com/reaction/1499721

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 h. After cooled to rt, the mixture was diluted with EtOAc and 1 N HCl. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with water, then brine and dried over magnesium sulfate, then concentrated to dry under reduced pressure. The residue was used directly in 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 numberUS09199982B2
Source datasetuspto-grants-2015_12
ORD IDord-e8510ea7f3e140e1aaafa95a34f28f58
Source noteuspto-grants-2015_12