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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46556Generated: October 25, 2026

Sodium Cyanide → 3,4-Difluorobenzoylacetonitrile

https://huagongshe.com/reaction/46556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant2-Bromo-1-(3,4-difluorophenyl)ethan-1-oneHCID 2737032—
Reactant3-Oxo-3-(4-(propan-2-yl)phenyl)propanenitrileHCID 4352886—
Reactant3-(2,5-Difluorophenyl)-3-oxopropanenitrileHCID 12540175—
Reactant3-(2,4-Dichlorophenyl)-3-oxopropanenitrileHCID 13630728—
Reactantm-IsobutylbenzoylacetonitrileHCID 20387494—
Reactant3-(3,4-Dimethylphenyl)-3-oxopropanenitrileHCID 20387502—
Reactant3-(3-Ethoxyphenyl)-3-oxopropanenitrileHCID 20387504—
Reactant3,4-DiethoxybenzoylacetonitrileHCID 20387507—
Reactant3-(2-Ethyl-phenyl)-3-oxo-propionitrileHCID 20387509—
Reactant4-(1-Methylethoxy)-beta-oxobenzenepropanenitrileHCID 20387514—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3,4-DifluorobenzoylacetonitrileHCID 2758254—

Reaction Steps

A solution of 13.2 g. (0.056 mole) of 3,4-difluorophenacyl bromide was dissolved in 100 ml. of ethanol and cooled to 5° C. in ice. A solution of 7.6 g. (0.16 mole) of sodium cyanide in 40 ml. of water was added dropwise over 0.5 hr. and the reaction is stirred for an additional one hour. At that time, the mixture was diluted with 100 ml. of water and filtered through Celite®. Acidification of the filtrate gave a cloudy mixture which was extracted with methylene chloride. The organic phase was dried, filtered through Magnesol® and evaporated. Recrystallization of the residue from carbon tetrachloride provides 5.3 g. (52%) of colorless solid, m.p. 74°-75° C. Similarly prepared were 2,4-dichlorobenzoylacetonitrile, o-ethylbenzoylacetonitrile, p-isopropylbenzoylacetonitrile, m-isobutylbenzoylacetonitrile, 3,4-dimethylbenzoylacetonitrile, m-ethoxybenzoylacetonitrile, p-isopropoxybenzoylacetonitrile, 3,4-diethoxybenzoylacetonitrile, and 2,5-difluorobenzoylacetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04173650
Source datasetuspto-grants-1979_11
ORD IDord-46c5ea2bab6c41c3b7fdd1b63e77ae47
Source noteuspto-grants-1979_11