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HRID 584352作成日:2026年10月26日

Triethylamine → m-Phenoxybenzyl cyanide

https://huagongshe.com/reaction/584352

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Phenoxybenzyl alcoholHCID 26295—
溶媒Ethyl AcetateHCID 8857—
溶媒Methanesulfonyl chlorideHCID 31297—
生成物m-Phenoxybenzyl cyanideHCID 4007532%

反応手順

To a solution of 3-phenoxybenzylalcohol (25.0 g) and triethylamine (26.3 ml) in ethyl acetate (300 ml), methanesulfonyl chloride (14.6 ml) was added dropwise at 0° C. After stirring for 1 hour, the reaction mixture was washed with saturated aqueous sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in acetone (300 ml), admixed with sodium iodide (37.5 g) and then stirred for 1 hour. The reaction mixture was concentrated, and the residue was diluted with water and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and then concentrated. The residue was dissolved in dimethyl sulfoxide (100 ml) and stirred with sodium cyanide (7.35 g) for 15 hours at room temperature. The reaction mixture was diluted with ethyl acetate, washed with water, dried (MgSO4), and then concentrated. The residue was subjected to column chromatography on silica gel to obtain 3-phenoxyphenylacetonitrile (8.36 g, yield 32%) as an oil from a fraction eluted with ethyl acetate-hexane (1:7. v/v).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06924300B2
出典データセットuspto-grants-2005_08
ORD IDord-641bab9e2a0943d386ef1cd4bfeb9dbd
出典メモuspto-grants-2005_08