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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730043Generated: November 3, 2026

Ammonia → HCID 21421755, compound

https://huagongshe.com/reaction/1730043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthanolHCID 702—
ReactantHCID 178513758HCID 178513758—
CatalystNickelHCID 935—
ProductHCID 21421755HCID 21421755—

Reaction Steps

To 80 parts of ethanol, previously saturated with gaseous ammonia, are added 2.3 parts of (-)-2-mercapto-1-(2-phenylethyl)-1H-imidazole-5-carboxamide hydrate and 6 parts of Raney-nickel. The mixture is stirred and refluxed for 2 hours and thereafter allowed to cool to room temperature. The Raney-nickel is filtered off and the filter-cake is washed with ethanol. The filtrate is evaporated in vacuo and the residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol and eluent. The pure fractions are collected and the eluent is evaporated, yielding (-)-1-(1-phenylethyl)-1H-imidazole-5-carboxamide, essentially free of its (+)-isomer, as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991072
Source datasetuspto-grants-1976_11
ORD IDord-723dc4c2eb7040ffb2b8ff581d839afd
Source noteuspto-grants-1976_11