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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760014Generated: November 1, 2026

Cyanide → (3-Methoxy-5-methylphenyl)acetonitrile

https://huagongshe.com/reaction/1760014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanideHCID 5975—
ReactantAcetonitrileHCID 6342—
ReactantSodium CyanideHCID 8929—
Reactant1-(Bromomethyl)-3-methoxy-5-methylbenzeneHCID 585534—
SolventDimethyl SulfoxideHCID 679—
Product(3-Methoxy-5-methylphenyl)acetonitrileHCID 2204824170%

Reaction Steps

To a solution of 3-bromomethyl-5-methylanisole (17 g; 0.008 mol; from step (i) above) in DMSO (25 mL) was added NaCN (8.2 g; 0.16 mol). The mixture, which became very warm upon the addition of the cyanide, was left to cool to room temperature over 1 hour. CH3CN (25 mL) was then added, and the mixture refluxed for 1 hour. The reaction mixture was concentrated, water (200 mL) was added, and the resultant solution was extracted 3 times with ether. The combined organic phase was washed with water, dried (Na2SO4), and concentrated to give 9 g (70%) of the sub-title product as a yellow oil, which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838478B2
Source datasetuspto-grants-2005_01
ORD IDord-c2198b3dc0d5438c831245d3c5f63542
Source noteuspto-grants-2005_01