HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-1,1,1-trifluoro-2-propanone → 4-Methyl-1-(4-trifluoromethyl-2-thiazolyl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-1,1,1-trifluoro-2-propanone | HCID 79008 | — |
| Reactant | 4-Methylpiperazine-1-carbothioamide | HCID 2113086 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methyl-1-(4-trifluoromethyl-2-thiazolyl)-piperazine | HCID 13747809 | — |
Reaction Steps
To a solution of 33.9 g 1-bromo-3,3,3-trifluoro-2-propanone in 300 ml of absolute ethanol are added 28.6 g 4-methyl-1-piperazinylthiocarboxamide. The mixture is refluxed for 4 hours, evaporated to dryness and the residue partitioned between ethyl ether and aqueous NaOH. The ether phase is washed, dried and evaporated, whereby the title compound is obtained, m.p. 62° (ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892879 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-688ebc6358ea41d4909a6f288fb7d236 |
| Source note | uspto-grants-1990_01 |