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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429793Generated: October 30, 2026

Benzyl Alcohol → Phenylacetonitrile

https://huagongshe.com/reaction/429793

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 numberUS06319928B1
Source datasetuspto-grants-2001_11
ORD IDord-cd8e5fb196eb4634b11f5b55fbaff037
Source noteuspto-grants-2001_11