HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 20354921, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | HCID 178455594 | HCID 178455594 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20354921 | HCID 20354921 | — |
Reaction Steps
A mixture of 9.5 g. 3-sec.butylsulphonyl-1,2,4-triazole, 7.97 g. diallylcarbamoyl chloride, 50 ml. dry tetrahydrofuran and 7.5 ml. dry triethylamine was refluxed under anhydrous conditions for 5 hours. The reaction mixture was worked up by a method analogous to that described in Example 1 to give an oil which was not distilled but was heated under reduced pressure. (95°C/0.1 mm.) for 4 hours to remove traces of volatile material. The resulting product, 1-diallylcarbamoyl-3-sec.butylsulphonyl-1,2,4-triazole, was obtained as an oil, nD26 1.5174. (98.9% 1-isomer by GLC assay). Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952001 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-926e64caf9134cd7abd9e201cc02a51e |
| Source note | uspto-grants-1976_04 |