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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627366Generated: October 30, 2026

3-(3-Bromo-4-fluorophenyl)-3-methylbutan-2-one → 2-Fluoro-5-(2-methyl-3-oxobutan-2-yl)benzonitrile

https://huagongshe.com/reaction/1627366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Bromo-4-fluorophenyl)-3-methylbutan-2-oneHCID 66740799—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Fluoro-5-(2-methyl-3-oxobutan-2-yl)benzonitrileHCID 6674093169.2%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a solution of 3-(3-bromo-4-fluorophenyl)-3-methylbutan-2-one (13 g, 50 mmol) in NMP (100 mL) was added CuCN (17.9 g, 200 mmol, 4 eq). The mixture was heated 24 h at 160° C. After cooling, the reaction was diluted with EtOAc, washed with 2N HCl (200 mL), satd NaHCO3 (200 mL) and brine (200 mL) successively, dried over MgSO4 and evaporated in vacuo. The residue was purified by column chromatography (Hex/EtOAc=4:1) to give 2-fluoro-5-(2-methyl-3-oxobutan-2-yl)benzonitrile (7.1 g, 69%). 1H NMR (400 MHz, CDCl3) δ 7.56-7.54 (m, 1H), 7.49-7.45 (m, 1H), 7.20 (t, J=8.4 Hz, 1H), 1.96 (s, 3H), 1.50 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785488B2
Source datasetuspto-grants-2014_07
ORD IDord-2f36a35aaf084f03b95342fee5c95d4f
Source noteuspto-grants-2014_07