Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526076Generated: October 26, 2026

Sodium Cyanide → 2-(2-Methylpyridin-3-yl)acetonitrile

https://huagongshe.com/reaction/1526076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(Chloromethyl)-2-methylpyridineHCID 12243711—
SolventDimethylformamideHCID 6228—
Product2-(2-Methylpyridin-3-yl)acetonitrileHCID 19099286—

Reaction Conditions

Temperature45 °C

Reaction Steps

970 mg (6.85 mmol) of the compound from Example 37A are initially introduced into 10 ml DMF, 336 mg (6.85 mmol) sodium cyanide are added and the mixture is stirred overnight at 45° C. The reaction mixture is introduced on to 75 ml saturated ammonium chloride solution and extracted several times with methylene chloride. The combined organic phases are dried over sodium sulfate, filtered and concentrated. The residue is purified by means of flash chromatography on silica gel (mobile phase: methylene chloride/methanol 20:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085572B2
Source datasetuspto-grants-2015_07
ORD IDord-07f501c867bc41e79921de518d0fc9c5
Source noteuspto-grants-2015_07