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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500340Generated: October 29, 2026

Water → 2-Cyano-5-methoxybenzeneacetonitrile

https://huagongshe.com/reaction/500340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CyanideHCID 9032—
Reactant28970-91-4HCID 12668051—
SolventEthanolHCID 702—
Product2-Cyano-5-methoxybenzeneacetonitrileHCID 59423525—

Reaction Steps

2-(Bromomethyl)-4-methoxybenzonitrile (36 g, example 235, step 1) was suspended in 200 ml of ethanol, 200 ml of acetonitrile was added followed by KCN (8.3 g) and 150 ml of water. Mixture was stirred and the colorless solution turned to yellow. The reaction was complete after 4 hours of stirring. The volatiles were removed under vacuum, and the residual solid was redissolved in ethyl acetate (200 ml) and washed with water (100 ml) and brine (100 ml). The organics were then dried over sodium sulfate. Ethyl acetate was removed and the residue was recrystallized from ethyl acetate and dichloride methane to provide 17 g of 2-(cyanomethyl)-4-methoxybenzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772180B2
Source datasetuspto-grants-2010_08
ORD IDord-7954d7c1b7084f48809115a2ba5e4db6
Source noteuspto-grants-2010_08