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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501632Generated: October 30, 2026

N-(4-Bromo-3-fluoro-2-methylphenyl)acetamide → N-(4-Cyano-3-fluoro-2-methylphenyl)acetamide

https://huagongshe.com/reaction/501632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Bromo-3-fluoro-2-methylphenyl)acetamideHCID 67123438—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
ProductN-(4-Cyano-3-fluoro-2-methylphenyl)acetamideHCID 6845496888.7%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of N-(4-bromo-3-fluoro-2-methylphenyl)acetamide (72B) (2.18 g, 8.86 mmol) in DMF (20 mL) was added CuCN (2.61 g, 29.1 mmol). The mixture was stirred at 150° C. for 12 h and was then poured into ice (50 g). After warming to rt, the product was extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine, dried and concentrated. The residue was purified via flash chromatography eluting with a solution of 5% methanol in 95% of EtOAc/hexane (1:1) to provide the title compound (1.51 g) as a white solid. LCMS: m/z 193 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772267B2
Source datasetuspto-grants-2010_08
ORD IDord-1f5ff80f4127475683e68f12bebfbd56
Source noteuspto-grants-2010_08