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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742096Generated: October 30, 2026

N,N-Dimethylaniline → HCID 178423881, compound

https://huagongshe.com/reaction/742096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantCyanogenHCID 9999—
Reactant2-Amino-1-(4-methylphenyl)ethan-1-one hydrochlorideHCID 12487186—
SolventDimethylformamideHCID 6228—
ProductHCID 178423881HCID 17842388170%

Reaction Conditions

Temperature100 °C

Reaction Steps

15 g (81 mmol) of 2-amino-4'-methylacetophenone hydrochloride was measured out in a 200-ml four-necked flask. To the material was then added 121 ml (121 mmol) of a 1 mol/l N,N-dimethylformamide solution of cyanogen. The mixture was then stirred. To the mixture was then added 29.4 g (243 mmol) of N,N-dimethylaniline. The mixture was then heated at a temperature of 100° C. with stirring for 3 hours. N,N-dimethylaniline was then distilled off from the reaction mixture under a pressure of 30 mmHg. The reaction mixture was then allowed to cool to room temperature. 200 ml of water was then poured into the reaction mixture. The reaction mixture was acidified with hydrochloric acid, and a precipitate was recovered by filtration. The filtration residue was dissolved in 200 ml of a 5% aqueous solution of sodium hydroxide, and the solution was filtered. The filtrate was then acidified with hydrochloric acid. 2-Cyano-4-(p-tolyl)imidazole as a desired compound was then recovered by filtration. The material was then dried to obtain 12.43 g of a desired compound with a purity of 83.4% (yield: 70.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552557
Source datasetuspto-grants-1996_09
ORD IDord-086e7efb4a5c4d05b5c09c14a36791fc
Source noteuspto-grants-1996_09