HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20290106, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | ethyl(isopropyl)carbaMic chloride | HCID 21185221 | — |
| Reactant | HCID 178496539 | HCID 178496539 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20290106 | HCID 20290106 | — |
Reaction Steps
A solution of 0.03 mole of 3-(2-methoxyethylsulphonyl)-1,2,4-triazole, 6 ml. of triethylamine and 0.033 mole of N-ethyl-N-isopropylcarbamoyl chloride in 40 ml. of dry tetrahydrofuran was heated under reflux for 15 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated to remove solvent. The product crystallized on cooling and treatment with 100 ml. of petroleum ether (b.p. 62°-68°C). This solid was collected and recrystallized from 100 ml. benzene/ petroleum ether (b.p. 40°-60°C) to give 1-(N-ethyl-N-isopropylcarbamoyl)-3-(2-methoxyethylsulphonyl)-1,2,4-triazole, m.p. 64°-65°C. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952001 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-c87d7e10935e439b93f3c03fb5964875 |
| Source note | uspto-grants-1976_04 |