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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862998Generated: October 26, 2026

Butyl Chloride → 2-(4-Phenylthiophenyl) hexanenitrile

https://huagongshe.com/reaction/1862998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl ChlorideHCID 8005—
ReactantSodium HydroxideHCID 14798—
Reactant[4-(Phenylsulfanyl)phenyl]acetonitrileHCID 238605—
CatalystTetraethylammonium BromideHCID 6285—
SolventWaterHCID 962—
Product2-(4-Phenylthiophenyl) hexanenitrileHCID 5442298065.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167576
Source datasetuspto-grants-1979_09
ORD IDord-33d9bcc835934a3f8b1fef328e275a04
Source noteuspto-grants-1979_09