HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Diallylcarbamoyl-3-propylthio-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diallylcarbamyl chloride | HCID 3449313 | — |
| Reactant | HCID 178460806 | HCID 178460806 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Diallylcarbamoyl-3-propylthio-1,2,4-triazole | HCID 20355094 | — |
Reaction Steps
A mixture of 5.75 g. 3-propylthio-1,2,4-triazole, 6.8 g. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 8 ml. dry triethylamine was refluxed under anhydrous conditions for 3 hours. The reaction mixture was worked up as described in Example 1 to produce an oil which was distilled under reduced pressure to give 1-diallylcarbamoyl-3-propylthio-1,2,4-triazole, b.p. 134° - 135° C./0.1 mm. Gas-liquid chromatographic (GLC) assay indicated a content of 1-isomer of 94.2%. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087269 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-75c2f898eb4e42d580103087a09f1e8d |
| Source note | uspto-grants-1978_05 |