HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Diallylcarbamoyl-3-isopropylsulphonyl-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | HCID 178461014 | HCID 178461014 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Diallylcarbamoyl-3-isopropylsulphonyl-1,2,4-triazole | HCID 20355132 | — |
Reaction Steps
A mixture of 7.0 g. 3-isopropylsulphonyl-1,2,4-triazole, 7.0 ml. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 8 ml. dry triethylamine was refluxed for 1 hour under anhydrous conditions. The reaction mixture was worked up as described in Example 1 to give 1-diallylcarbamoyl-3-isopropylsulphonyl-1,2,4-triazole as an oil which was heated under reduced pressure (100° C./0.5 mm.) for 1 hour to remove all traces of volatile material. Refractive index of product nD26 1.5158. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087269 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-3ecac75819f34769b499d8b0869d11e9 |
| Source note | uspto-grants-1978_05 |