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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128224Generated: October 27, 2026

Butyl Chloride → 2-(4-Phenylthiophenyl) hexanenitrile

https://huagongshe.com/reaction/128224

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 numberUS04259339
Source datasetuspto-grants-1981_03
ORD IDord-1d8b680913c54b35923d1760dd742b70
Source noteuspto-grants-1981_03