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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262431Generated: October 26, 2026

Sodium Chloride → 4-Hydroxybenzyl cyanide

https://huagongshe.com/reaction/262431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium CyanideHCID 8929—
ReactantSodium 4-hydroxyphenylglycolateHCID 23663713—
Product4-Hydroxybenzyl cyanideHCID 26548—

Reaction Conditions

Temperature135 °C

Reaction Steps

Sodium cyanide (25.0 g.) is added to a stirred suspension of anhydrous sodium p-hydroxymandelate (96 g. of 99% w/w material, the impurity being sodium chloride; prepared from 104 g. of monohydrate by azeotropic distillation with 500 ml. of xylene in a Dean and Stark apparatus) in N,N-dimethylformamide (100 ml.), and the mixture is heated at 135° C. for 1 hour and then cooled. Water (170 ml.) and formic acid (38 ml.) are added and the mixture is extracted twice with methyl isobutyl ketone (330 ml. and 170 ml. respectively). The combined extracts are washed twice with water (240 ml. and 180 ml. respectively) and then concentrated by evaporation. There is thus obtained a solution of p-hydroxybenzyl cyanide in methyl isobutyl ketone which is suitable for conversion to p-hydroxyphenylacetamide without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154757
Source datasetuspto-grants-1979_05
ORD IDord-28aa4e4d450c4980b51e07ba96da11ab
Source noteuspto-grants-1979_05