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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448098Generated: October 31, 2026

N,N-Dimethylaniline → HCID 20298796, compound

https://huagongshe.com/reaction/1448098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantSodium amideHCID 24533—
ReactantHCID 20298827HCID 20298827—
ProductHCID 20298796HCID 20298796—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 4.1 parts of 5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-ethyl-1H-benzimidazole, 1.2 parts of sodium amide and 20 parts of N,N-dimethylbenzenamine is stirred and heated slowly to 135° C. Stirring at 135° C. is continued for 3 hours. The reaction mixture is cooled and poured onto water. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) and a small amount of ammonium hydroxide as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from methylbenzene. The product is filtered off and dried, yielding 1.5 parts of 5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-ethyl-1H-benzimidazol-2-amine; mp. 214.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179505
Source datasetuspto-grants-1979_12
ORD IDord-b51fa7eb80fb4831a18f81c9fb48b464
Source noteuspto-grants-1979_12