HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylcarbamoyl chloride → 1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178457344 | HCID 178457344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole | HCID 21324268 | — |
Reaction Steps
A mixture of 6.9 g. 3-diallylsulphamoyl-1,2,4-triazole, 4.5 g. diethylcarbamoyl chloride, 6ml. triethylamine and 25 ml. dry tetrahydrofuran was refluxed under anhydrous conditions for 1.5 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated to remove solvent. The solid residue was recrystallized from petroleum ether, b.p. 60°-80° C., to give 1-diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole, m.p. 49°-51° C. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148626 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-4267794288414405abf990af1d5262c8 |
| Source note | uspto-grants-1979_04 |