Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128228Generated: October 25, 2026

Butyl Chloride → 2-(3-Phenoxyphenyl)hexanenitrile

https://huagongshe.com/reaction/128228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl ChlorideHCID 8005—
ReactantSodium HydroxideHCID 14798—
Reactantm-Phenoxybenzyl cyanideHCID 40075—
CatalystTetraethylammonium BromideHCID 6285—
SolventWaterHCID 962—
Product2-(3-Phenoxyphenyl)hexanenitrileHCID 2346893354.8%

Reaction Steps

Into a three-necked 500 ml round-bottom flask are charged 35 g (0.17 mole) of m-phenoxybenzyl cyanide, 16.3 g (0.17 mole) of butyl chloride 4 g of tetraethylammonium bromide. To this mixture is added 27 g (0.34 mole) of 50% sodium hydroxide solution dropwise with stirring. The reaction mixture is heated at 90° for three hours. It is then poured into water and extracted with hexane. The combined hexane extracts are washed with water and dried over MgSO4. Solvent is evaporated to give 39 g of crude product. Vacuum distillation (149°-155°/0.2 mm) provides 24.7 g of pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259339
Source datasetuspto-grants-1981_03
ORD IDord-6d9cf5bcc342455dbac8b50fec879111
Source noteuspto-grants-1981_03