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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723132Generated: November 4, 2026

Imidazole → HCID 14518416, compound

https://huagongshe.com/reaction/1723132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantHCID 14518406HCID 14518406—
SolventAcetonitrileHCID 6342—
ProductHCID 14518416HCID 1451841654%

Reaction Steps

A mixture of 6.8 parts of 1H-imidazole, 4.9 parts of 5-(chloromethyl)-2-ethyl-1-methyl-1H-benzimidazole monohydrochloride and 80 parts of acetonitrile was stirred and refluxed for 3 hours. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from ethyl acetate. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 2.6 parts (54%) of 2-ethyl-5-(1H-imidazol-1-yl-methyl)-1-methyl-1H-benzimidazole; mp. 127.3° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859684
Source datasetuspto-grants-1989_08
ORD IDord-ca3003da746947ecbf2a288dfc12b1f9
Source noteuspto-grants-1989_08