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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389310Generated: October 29, 2026

N,N-Dimethylaniline → HCID 20298796, compound

https://huagongshe.com/reaction/1389310

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 numberUS04243806
Source datasetuspto-grants-1981_01
ORD IDord-58467af5afc24060b43c234e15911e00
Source noteuspto-grants-1981_01