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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 12833675 | HCID 12833675 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Butyl-5-(4-methoxyphenyl)-1H-imidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533550 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-e2e3d261a6004631acdf7f9a44ca5cd6 |
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| Source note | uspto-grants-1985_08 |
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