HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-1,2,4-Triazole → 4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-1-(4-chlorophenyl)-2-methylpropan-1-one | HCID 11299973 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone | HCID 13366855 | 25.7% |
Reaction Steps
80 g (0.31 mole) of 2-bromo-prop-2-yl 4-chlorophenyl ketone, 26.9 g (0.39 mole) of 1,2,4-triazole and 53.8 g (0.39 mole) of potassium carbonate are heated under reflux in 350 ml of acetone for 6 hours. The mixture is allowed to cool and is filtered and the filtrate is concentrated in vacuo. The residue is taken up in methylene chloride and the mixture is washed with water, dried over sodium sulphate and concentrated in vacuo. The residue is recrystallised from diisopropyl ether. 19.9 g (25.7% of theory) of 4-chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone of melting point 111° C. are obtained. ##STR19##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05011850 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-277a6eaca078433b9231c2c716a58751 |
| Source note | uspto-grants-1991_04 |