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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585554Generated: November 4, 2026

Benzyl Alcohol → Phenylacetonitrile

https://huagongshe.com/reaction/1585554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium CyanideHCID 9032—
ReactantThionyl ChlorideHCID 24386—
SolventDichloromethaneHCID 6344—
ProductPhenylacetonitrileHCID 8794195.4%

Reaction Conditions

Temperature52.5 °C

Reaction Steps

To a solution of 40.00 g (180 mmoles) of benzyl alcohol in 530 ml of dichloromethane was added within 5 min 32.7 ml (450 mmoles) of thionyl chloride. The solution was evaporated in vacuo to dryness, which was repeated after toluene addition: 46.30 g (106.9%) of crude benzyl chloride, which was dissolved in 230 ml of dimethylformamide and treated with 23.50 g (360 mmoles) of potassium cyanide. The mixture was heated for 4 hours to 50-55° C. The salt was filtered off and the filtrate evaporated in vacuo to dryness, which was repeated after the addition of water, the residue was taken up in ether and extracted with 1N NaOH. The ether phase is evaporated to dryness to yield 41.20 g (99.0%) of crude benzyl cyanide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939422
Source datasetuspto-grants-1999_08
ORD IDord-f92779a276a1484281b4de2b57461325
Source noteuspto-grants-1999_08