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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462150Generated: November 3, 2026

Sodium Cyanide → (4-tert-Butylphenyl)acetonitrile

https://huagongshe.com/reaction/1462150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantTetrabutylammoniumHCID 16028—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
SolventWaterHCID 962—
Product(4-tert-Butylphenyl)acetonitrileHCID 76784—

Reaction Steps

A mixture consisting of 107 g p-tert.butylbenzyl bromide, 2 g tetra butyl-ammonium jodide and 37 g NaCN in 50 ml water was heated during 1 hour at 100° C. After cooling the reaction mixture, the organic layer was separated and distilled in vacuo with a yield of 78 g of the desired cyanide. Then this product was fractionated in vacuo. Yield of p-tert.butylbenzyl cyanide: 65 g (80%): boiling point: 118° C./0,7 kPa: nD =1,5110. This cyanide has a very strong odor which reminds one of algae, seaweed and ozone with ambergris-like, fatty and animal notes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459224
Source datasetuspto-grants-1984_07
ORD IDord-af5034d7c5a44ebc89bd5ca9c40ceed5
Source noteuspto-grants-1984_07