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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484659Generated: October 29, 2026

Ammonium Hydroxide → 1-Butyl-5-(4-methoxyphenyl)-1H-imidazole

https://huagongshe.com/reaction/484659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 12833675HCID 12833675—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product1-Butyl-5-(4-methoxyphenyl)-1H-imidazoleHCID 20271733—

Reaction Steps

A mixture of 11 parts of 1-butyl-5-(4-methoxyphenyl)-2-(methylthio)-1H-imidazole monohydrochloride, 20 parts of Raney-nickel catalyst, 105 parts of ammonium hydroxide and 8 parts of methanol is stirred for 2 hours at room temperature. The Raney-nickel catalyst is filtered off and another 20 parts of Raney-nickel catalyst is added. The whole is stirred for another 2 hours at room temperature. The catalyst is filtered off and the filtrate is evaporated. The residue is taken up in a small amount of water and the product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 8 of 1-butyl-5-(4-methoxyphenyl)-1H-imidazole as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533550
Source datasetuspto-grants-1985_08
ORD IDord-e2e3d261a6004631acdf7f9a44ca5cd6
Source noteuspto-grants-1985_08