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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752374Generated: October 28, 2026

Benzoic Acid → cyanomethyl benzoate

https://huagongshe.com/reaction/1752374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantBromoacetonitrileHCID 11534—
SolventDimethylformamideHCID 6228—
Productcyanomethyl benzoateHCID 27777395%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 50.0 g (0.41 mol) benzoic acid in 150 mL N,N-dimethylformamide 70.0 g (0.50 mol) potassium carbonate was added and the mixture was stirred until the evolution of gas has ceased. The reaction mixture was cooled to 0° C. and a solution of 29.0 mL (0.41 mol) bromoacetonitrile in 50 mL N,N-dimethylformamide was added dropwise. The reaction mixture was stirred overnight at room temperature. The solvent was evaporated and the residue was dissolved in 500 mL ethyl acetate. It was washed with water (3×150 mL), saturated aqueous sodium hydrogencarbonate (150 mL) and brine. The organic layer was separated and dried over anhydrous sodium sulfate. The drying agent was filtered off and the solvent was evaporated. The resulting crude product was purified by column chromatography (hexane-ethyl acetate 9:1 to 4:1) to yield cyanomethyl benzoate 62.6 g (95%). 1H-NMR (400 MHz; DMSO-d6): 7.98 (m, 2H), 7.69 (m, 1H), 7.54 (m, 2H), 5.20 (s, 2H); GCMS for C9H7NO2: 161 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163006B2
Source datasetuspto-grants-2015_10
ORD IDord-73db3e5284ca43ada1b12e1902cb52e8
Source noteuspto-grants-2015_10