HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → HCID 20089150, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67790043 | HCID 67790043 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20089150 | HCID 20089150 | 69.2% |
Reaction Steps
To the solution of 3-(4-chlorophenyl)-4-ethyl-1,2,4-triazolin-5-one (2.23 g, 0.01 mole) in dry acetone (40 ml) was added, at room temperature, potassium carbonate (1.67 g, 0.0012 mole) followed by propargyl bromide (1.8 g of 80% in toluene, 0.012 mole). The reaction mixture was then refluxed with stirring for 6 hr. The mixture was cooled down to room temperature and solvent was evaporated to give a residue. The product was purified by crystallization from hexane/ether, affording 1.8 g (69.2% yield) of 1-propargyl-3-(4-chlorophenyl)-4-ethyl-1,2,4-triazolin-5-one as a white solid, m.p. 115°-119° C. A proton NMR spectrum was consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064845 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-8cd6989ac75e45e5b465b70322621518 |
| Source note | uspto-grants-1991_11 |