HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389310Generated: October 29, 2026
N,N-Dimethylaniline → HCID 20298796, compound
https://huagongshe.com/reaction/1389310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | HCID 20298827 | HCID 20298827 | — |
| Product | HCID 20298796 | HCID 20298796 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243806 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-58467af5afc24060b43c234e15911e00 |
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| Source note | uspto-grants-1981_01 |
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