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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448106Generated: November 3, 2026

Acetic Anhydride → HCID 131711667, compound

https://huagongshe.com/reaction/1448106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 19890747HCID 19890747—
SolventTolueneHCID 1140—
ProductHCID 131711667HCID 13171166774.4%

Reaction Steps

A mixture of 1.9 parts of 5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-methyl-1H-benzimidazole-2-methanol, 1.55 parts of acetic acid anhydride and 45 parts of methylbenzene is stirred and refluxed for 2 hours. The reaction mixture is cooled, washed with a diluted ammonium hydroxide solution and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from a mixture of methylbenzene and 2,2'-oxybispropane (20:20 by volume). The product is filtered off and dried, yielding 1.5 parts (74.4%) of {5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-methyl-1H-benzimidazol-2-ylmethyl}acetate; mp. 201.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179505
Source datasetuspto-grants-1979_12
ORD IDord-7b537ddc0ecf45fcae9726bd775bf79c
Source noteuspto-grants-1979_12