HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165138Generated: October 26, 2026
Hydrochloric Acid → 1-(4-Hydroxy-3,5-di-tert.-butylbenzoylamino)-2-methylimidazole
https://huagongshe.com/reaction/1165138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzoyl chloride | HCID 3787187 | — |
| Reactant | HCID 22167428 | HCID 22167428 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Hydroxy-3,5-di-tert.-butylbenzoylamino)-2-methylimidazole | HCID 19862532 | — |
Reaction Steps
1.0 g of 1-amino-2-methylimidazole hydrochloride and 2.0 g of 4-hydroxy-3,5-di-tert.-butylbenzoyl chloride are mixed and heated on an oil-bath for 40 minutes to 200°-210° (bath temperature), whereby the flask content melts with the evolution of HCl and then again becomes solid. The cooled flask content is dissolved in 30 ml of water, whereupon the solution is filtered and the filtrate is adjusted to pH 9 with 10% sodium carbonate solution. The separated precipitate is removed by filtration and dissolved in 25 ml of hot ethanol, whereupon the still hot solution is treated with 10 ml of water. After cooling, the separated solid is removed by filtration and recrystallized from ethyl acetate. There is obtained 1-(4-hydroxy-3,5-di-tert.-butylbenzoylamino)-2-methylimidazole of m.p. 322°-324° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04908363 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-adca8df6e9a64c83a6392a78506ddc84 |
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| Source note | uspto-grants-1990_03 |
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