Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822637Generated: November 2, 2026

Sodium Cyanide → 2-(2-tert-Butyl-1,3-oxazol-4-yl)acetonitrile

https://huagongshe.com/reaction/1822637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantSodium HydroxideHCID 14798—
Reactant2-tert-Butyl-4-(chloromethyl)-1,3-oxazoleHCID 22169510—
SolventDimethyl SulfoxideHCID 679—
Product2-(2-tert-Butyl-1,3-oxazol-4-yl)acetonitrileHCID 2216951792.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

6.2 g of sodium cyanide was weighed, 50 ml of dimethylsulfoxide was added thereto, and a dimethylsulfoxide solution of 16.9 g of 2-tert-butyl-4-chloromethyloxazole was dropwise added thereto, and heated on an oil bath at 65° C. for 1 hour with stirring. After the resulting product was cooled to room temperature, 150 ml of a dilute aqueous solution of sodium hydroxide was added thereto, and extracted with toluene. The organic layer was fully washed with water, and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 14.8 g of 2-tert-butyl-4-cyanomethyloxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037880B2
Source datasetuspto-grants-2006_05
ORD IDord-d2be63a45d7d4beeb106a96c4dcbcba1
Source noteuspto-grants-2006_05