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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1862998생성일: 2026년 10월 26일

Butyl Chloride → 2-(4-Phenylthiophenyl) hexanenitrile

https://huagongshe.com/reaction/1862998

반응식

참여 물질

역할이름HCID투입량
반응물Butyl ChlorideHCID 8005—
반응물Sodium HydroxideHCID 14798—
반응물[4-(Phenylsulfanyl)phenyl]acetonitrileHCID 238605—
촉매Tetraethylammonium BromideHCID 6285—
용매WaterHCID 962—
생성물2-(4-Phenylthiophenyl) hexanenitrileHCID 5442298065.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04167576
출처 데이터셋uspto-grants-1979_09
ORD IDord-33d9bcc835934a3f8b1fef328e275a04
출처 메모uspto-grants-1979_09