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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504944Generated: November 1, 2026

Ethyl Acetate → N-(4-cyano-2-fluoro-5-(trifluoromethyl)phenyl)acetamide

https://huagongshe.com/reaction/1504944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-[4-Bromo-2-fluoro-5-(trifluoromethyl)phenyl]acetamideHCID 23274446—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
ProductN-(4-cyano-2-fluoro-5-(trifluoromethyl)phenyl)acetamideHCID 6829202856.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of compound 23 (300 mg, 1 mmol), CuCN (355 mg, 4 mmol) in DMF (6 mL) was heated at 150° C. under N2 overnight. The reaction mixture was cooled to room temperature and then poured into ice water. EtOAc was added and the insoluble solid was filtered off (rinsed with EtOAc). The organic layer was separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with aq.NaHCO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified with silica gel chromatography (PE:EtOAc=4:1) to afford the title compound 24 (140 mg, 28%) as a white solid. 1H NMR (400 MHz, CDCl3) δ8.99 (d, 1H, J=7.2 Hz), 7.55 (d, 1H, J=10.0 Hz), 2.92 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216957B2
Source datasetuspto-grants-2015_12
ORD IDord-fde8eaaa87d243409581d7a5eada02e4
Source noteuspto-grants-2015_12