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HRID 46556作成日:2026年10月23日

Sodium Cyanide → 3,4-Difluorobenzoylacetonitrile

https://huagongshe.com/ja/reaction/46556

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CyanideHCID 8929—
反応物2-Bromo-1-(3,4-difluorophenyl)ethan-1-oneHCID 2737032—
反応物3-Oxo-3-(4-(propan-2-yl)phenyl)propanenitrileHCID 4352886—
反応物3-(2,5-Difluorophenyl)-3-oxopropanenitrileHCID 12540175—
反応物3-(2,4-Dichlorophenyl)-3-oxopropanenitrileHCID 13630728—
反応物m-IsobutylbenzoylacetonitrileHCID 20387494—
反応物3-(3,4-Dimethylphenyl)-3-oxopropanenitrileHCID 20387502—
反応物3-(3-Ethoxyphenyl)-3-oxopropanenitrileHCID 20387504—
反応物3,4-DiethoxybenzoylacetonitrileHCID 20387507—
反応物3-(2-Ethyl-phenyl)-3-oxo-propionitrileHCID 20387509—
反応物4-(1-Methylethoxy)-beta-oxobenzenepropanenitrileHCID 20387514—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物3,4-DifluorobenzoylacetonitrileHCID 2758254—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04173650
出典データセットuspto-grants-1979_11
ORD IDord-46c5ea2bab6c41c3b7fdd1b63e77ae47
出典メモuspto-grants-1979_11