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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906168Generated: November 1, 2026

Water → Methyl 4-cyano-2-fluorobenzoate

https://huagongshe.com/reaction/906168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromo-2-fluoro-benzoic acid methyl esterHCID 11345311—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
ProductMethyl 4-cyano-2-fluorobenzoateHCID 1527872684%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of methyl 4-bromo-2-fluorobenzoate (9.1 mmol) in DMF (50 mL) was added zinc cyanide (641 mg, 5.5 mmol) followed by tetrakis(triphenyphosphine)palladium(0) (1.05 g, 0.91 mmol). The mixture was heated to 100° C. and stirred for 3 h. At that point, additional tetrakis(triphenyphosphine)-palladium(0) (500 mg, 0.43 mmol) was added. The mixture was stirred a further 30 min and was then cooled to room temperature. Water and ethyl acetate were added, and insoluble solids were removed by filtration through celite. The layers were then separated. The aqueous phase was extracted with ethyl acetate. The organic extracts were combined, washed with 10% aqueous lithium chloride, dried over magnesium sulfate, filtered and concentrated. The residue was purified by column chromatography (10% ethyl acetate in hexanes) to provide methyl 4-cyano-2-fluorobenzoate (1.36 g, 7.6 mmol, 84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-88d57607c9714ce489e3d884718b5e7a
Source noteuspto-grants-2011_09