戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1029818作成日:2026年10月27日

Sodium Cyanide → 2-Amino-2-benzyl-3-phenoxy-propionitrile

https://huagongshe.com/reaction/1029818

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Sodium SulfateHCID 24436—
反応物PhenoxyacetonitrileHCID 241641—
反応物HCID 178419663HCID 178419663—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-2-benzyl-3-phenoxy-propionitrileHCID 139832726.3%

反応手順

To 20 millimoles (2.66 g) of phenoxyacetonitrile in 6 ml of anhydrous ether, is added a solution of 30 millimoles (1.5 eg) of benzylmagnesium bromide in 6 ml of anhydrous ether. The mixture sets to a mass and 10 ml of tetrahydrofuran are added. After stirring for 2 hours at room temperature, the reaction mixture is cooled by an ice-bath, then added with 50 ml of a normal solution of sodium cyanide in dimethylformamide. After 2 hours of stirring at room temperature, the mixture is hydrolyzed by 10 ml of methanol then by pasty sodium sulfate. There are obtained 3.45 g of raw product, which purified by high pressure liquid chromatography on silica, with a solution by ethyl acetate/petroleum ether 1/1, give 0.3 g of 2-amino-2-benzyl-3-phenoxy-propionitrile. Yield: 6.3%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05103019
出典データセットuspto-grants-1992_04
ORD IDord-d79c602fcd994572be212c82ce10cf57
出典メモuspto-grants-1992_04