HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-acetylamino-1-(o-chlorobenzyl)-1H-1,2,3-triazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-amino-1-[(2-chlorophenyl)methyl]-1H-1,2,3-triazole-4-carboxamide | HCID 2815312 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-acetylamino-1-(o-chlorobenzyl)-1H-1,2,3-triazole-4-carboxamide | HCID 21282598 | — |
Reaction Steps
10,1 g of 5-amino-1-(o-chlorobenzyl)-1H-triazole-4-carboxamide are added, portionwise with stirring, to a mixture of 30,7 g of acetanhydride and 0,1 ml of sulphuric acid and heated to 60° . Stirring is continued for additional 30 minutes at 60° to 70° , the reaction mixture is poored into 250 ml of ethanol, heated to reflux for 30 minutes and evaporated in vacuo to dryness. The residue is triturated with 250 ml of ethyl acetate, the crystalline precipitate is collected and re-crystallised from ethyl acetate yielding 5-acetylamino-1-(o-chlorobenzyl)-1H-1,2,3-triazole-4-carboxamide of m.p. 181°-183°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04789680 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-72fec188baa94a90bba1a455e65c2b69 |
| Source note | uspto-grants-1988_12 |