HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Diallylcarbamoyl-3-ethylsulphonyl-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | HCID 178477666 | HCID 178477666 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Diallylcarbamoyl-3-ethylsulphonyl-1,2,4-triazole | HCID 20355134 | — |
Reaction Steps
A mixture of 6.45 g. 3-ethylsulphonyl-1,2,4-triazole, 6.6 g. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 8 ml. dry triethylamine was refluxed under anhydrous conditions for 1.5 hours. The cooled reaction mixture was filtered and the filtrate distilled under reduced pressure to remove solvent and give a product which distilled at 187° C./0.2 mm. This product solidified and was recrystallized from petroleum ether (b.p. 60° - 80° C.) to give 1-diallylcarbamoyl-3-ethylsulphonyl-1,2,4-triazole, m.p. 39° - 42° C. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087269 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-b034d7629ba14ffa9a5cf825914d638a |
| Source note | uspto-grants-1978_05 |