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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128222Generated: October 26, 2026

Butyl Chloride → 2-(2-Phenoxyphenyl)hexanenitrile

https://huagongshe.com/reaction/128222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl ChlorideHCID 8005—
ReactantSodium CyanideHCID 8929—
ReactantSodium HydroxideHCID 14798—
ReactantBenzene, (chloromethyl)phenoxy-HCID 169302—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-(2-Phenoxyphenyl)hexanenitrileHCID 1977561492.8%

Reaction Steps

Into a three-necked 300 ml round-bottom flask are charged 7.4 g (0.15 mole) of sodium cyanide and 80 ml of dimethyl sulfoxide. To this slurry is added 30 g (0.13 mole) of 2-phenoxybenzyl chloride dropwise. Reaction temperature increases from 24° to 44° C. The reaction mixture is stirred for an additional 11/2 hours. To this reaction mixture is added 13.7 g (0.13 mole) of butyl chloride followed by dropwise addition of 34 g (0.4 mole) of 50% sodium hydroxide solution. After stirring for an additional 1/2 hour, reaction mixture is poured into 150 ml of water and extracted with hexane. The combined hexane extracts are washed with water and dried over MgSO4. Solvent is evaporated to give 32 g of crude product. Material can be further purified by vacuum distillation (bp 149-60/0.25 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259339
Source datasetuspto-grants-1981_03
ORD IDord-992cbbc8a9db43cab0509ab776a9b49f
Source noteuspto-grants-1981_03