HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-1,2,4-Triazole → 4-(2,4-Dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-(2,4-dichlorophenyl)-3,3-dimethyl-2-butanone | HCID 13340381 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(2,4-Dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butanone | HCID 13340382 | — |
Reaction Steps
30 g (0.09 mol) of 1-bromo-4-(2,4-dichlorophenyl)-3,3-dimethyl-2-butanone, 12.4 g (0.18 mol) of 1,2,4-triazole and 24.8 g (0.18 mol) of potassium carbonate are heated under reflux in 300 ml of acetone for 6 hours. The mixture is then allowed to cool and is filtered with suction and the mother liquor 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 recrystallized from diethyl ether. 12.8 g (45.6% of theory of 4-(2,4-dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanone of melting point 85° C. are obtained. ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04870092 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-6a70b7160763427f9348c22b6fa8234e |
| Source note | uspto-grants-1989_09 |