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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863002Generated: October 26, 2026

Butyl Chloride → 2-(3-Phenoxyphenyl)hexanenitrile

https://huagongshe.com/reaction/1863002

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 numberUS04167576
Source datasetuspto-grants-1979_09
ORD IDord-cd0730cc712c4338ae854e988300bbda
Source noteuspto-grants-1979_09