HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165145Generated: November 1, 2026
Hydrochloric Acid → HCID 135984370, compound
https://huagongshe.com/reaction/1165145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
| Reactant | HCID 21782447 | HCID 21782447 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135984370 | HCID 135984370 | — |
Reaction Steps
0.65 g of 1-amino-2-methylmercaptoimidazole are dissolved in 50 ml of methanol and treated with 3 ml of 2N hydrochloric acid. After the addition of 1.05 g of 4-hydroxy-3,5-di-tert.-butylbenzaldehyde, the reaction mixture is stirred at room temperature overnight. Subsequently, the solvent is removed by evaporation in a vacuum. The residue is suspended in 30 ml of water and treated with saturated sodium carbonate solution up to an alkaline reaction. The mixture is extracted three times with 20 ml of methylene chloride each time, the combined organic phases are dried over sodium sulfate, filtered and evaporated. The crystalline residue is recrystallized from water/methanol, and there is obtained 1-(4-hydroxy-3,5-di-tert.-butylbenzylideneamino)-2-methylmercaptoimidazole of m.p. 181°-183°.
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-9eed381bae3e4c9c874d3f97c9688e63 |
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| Source note | uspto-grants-1990_03 |
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