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HRID 1862998作成日:2026年10月27日

Butyl Chloride → 2-(4-Phenylthiophenyl) hexanenitrile

https://huagongshe.com/reaction/1862998

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl ChlorideHCID 8005—
反応物Sodium HydroxideHCID 14798—
反応物[4-(Phenylsulfanyl)phenyl]acetonitrileHCID 238605—
触媒Tetraethylammonium BromideHCID 6285—
溶媒WaterHCID 962—
生成物2-(4-Phenylthiophenyl) hexanenitrileHCID 5442298065.1%

反応手順

To a mixture of 41 g (0.18 mole) of 4-phenylthiobenzyl cyanide, 18 g (0.19 mole) of butyl chloride and 2 g of tetraethylammonium bromide is added 16 g (0.2 mole) of 50% sodium hydroxide solution dropwise at room temperature with stirring. The reaction mixture is heated at 85° for 1/2 hour and then an additional 16 g (0.2 mole) of 50% sodium hydroxide solution are added. Heating is continued for another 1/2 hour. The reaction mixture is poured into water and extracted with ether. The combined ether extracts are washed with water, saturated sodium chloride solution and dried over MgSO4. Solvent is evaporated to give 47 g of a crude product. Vacuum distillation (173°-180°/0.05 mm) gives 33 g of pure product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04167576
出典データセットuspto-grants-1979_09
ORD IDord-33d9bcc835934a3f8b1fef328e275a04
出典メモuspto-grants-1979_09