HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Diallylcarbamoyl-3-butylsulphonyl-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | 3-Butylsulphonyl-1,2,4-triazole | HCID 178455595 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Diallylcarbamoyl-3-butylsulphonyl-1,2,4-triazole | HCID 20354976 | — |
Reaction Steps
A mixture of 5.7 g. 3-butylsulphonyl-1,2,4-triazole, 5.3 g. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 6 ml. dry triethylamine was refluxed under anhydrous conditions for 1.5 hours. The reaction mixture was worked up as described in Example 1 to give 1-diallylcarbamoyl-3-butylsulphonyl-1,2,4-triazole as an oil which was heated under reduced pressure (100° C./0.5 mm.) for 30 minutes to remove all traces of volatile material. Refractive index of product nD26 1.5132. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087269 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-5b1d710ba0bc49a789e9ed4311dc6d58 |
| Source note | uspto-grants-1978_05 |