HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 20354997, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | HCID 178455553 | HCID 178455553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20354997 | HCID 20354997 | — |
Reaction Steps
A mixture of 5.76 g. 3-sec.butylsulphinyl-1,2,4-triazole, 5.31 g. diallylcarbamoyl chloride, 50 ml. dry tetrahydrofuran and 5 ml. dry triethylamine was kept under anhydrous conditions at room temperature for 72 hours. The reaction mixture was filtered and the filtrate evaporated under reduced pressure at room temperature to give a residual oil which was dissolved in methylene dichloride. The resulting solution was washed with water, dried over anhydrous sodium sulphate and distilled under reduced pressure at room temperature to give 1-diallylcarbamoyl-3-sec.butylsulphinyl-1,2,4-triazole as a residual oil, nD25 1.5268, for which a satisfactory elemental analysis was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087269 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-7b499f774313477dac3fe81e8ed51225 |
| Source note | uspto-grants-1978_05 |