HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359694Generated: October 28, 2026
Acetic Anhydride → HCID 14459117, compound
https://huagongshe.com/reaction/359694
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14459112 | HCID 14459112 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 14459117 | HCID 14459117 | 55% |
Reaction Steps
1.4 g of acetic acid anhydride are added to 2.5 ml of formic acid, and the mixture is stirred at 60° C. for 30 minutes. The reaction solution is cooled in an ice bath, a solution of 1.07 g of 1-(4,6-dimethyl-2-pyridyl)-2-(2-aminobenzylthio)imidazole in 4 ml of formic acid is added thereto, and the mixture is stirred at room temperature for 1 hour. After the reaction, the solvent is distilled off. Water is added to the residue, and the aqueous mixture is made alkaline with potassium carbonate. The mixture is then extracted with ethyl acetate, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; ethyl acetate:n-hexane=1:1). The crude crystals obtained above are recrystallized from a mixture of ethyl acetate and n-hexane, whereby 0.64 g of 1-(4,6-dimethyl-2-pyridyl)-2-(2-formylaminobenzylthio)imidazole is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05002945 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-8cca76ebc1754a7f88f823f18489db27 |
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| Source note | uspto-grants-1991_03 |
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