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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783298Generated: November 1, 2026

Dimethylformamide → 2-Cyanomethyl-5-methylbenzamide

https://huagongshe.com/reaction/1783298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(Cyanomethyl)-5-methylbenzoic acidHCID 23084810—
SolventTetrahydrofuranHCID 8028—
Product2-Cyanomethyl-5-methylbenzamideHCID 23084702—

Reaction Steps

2-Cyanomethyl-5-methylbenzoic acid (16.3 g) and dimethylformamide (0.1 mL) were suspended in tetrahydrofuran (160 mL), and oxalyl dichloride (12.2 mL) was added dropwise under ice-cooling. After cease of foaming, the solvent was evaporated. The obtained residue was dissolved in tetrahydrofuran, and the solution was added dropwise to 28% aqueous ammonia solution under ice-cooling. After the completion of the reaction, the solvent was evaporated, and the precipitated crystals were collected by filtration to give 2-cyanomethyl-5-methylbenzamide (10.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501412B2
Source datasetuspto-grants-2009_03
ORD IDord-5302a0223cf146c2a418b84a39eda23c
Source noteuspto-grants-2009_03