HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Bromo-1-(2,4,6-trichlorophenyl)-3-(trifluoromethyl)-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | (2,4,6-Trichlorophenyl)hydrazine | HCID 79234 | — |
| Reactant | 3-Buten-2-one, 3-bromo-4-ethoxy-1,1,1-trifluoro- | HCID 3729078 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-1-(2,4,6-trichlorophenyl)-3-(trifluoromethyl)-1H-pyrazole | HCID 14274193 | 30.4% |
Reaction Steps
2.3 g (0.01 mole) of 3-bromo-4-ethoxy-1,1,1-trifluorobut-3-en-2-one are added to a solution of 4.2 g (0.02 mol) of 2,4,6-trichlorophenyl-hydrazine in 100 ml of ethanol which contains 0.01 mole hydrogen bromide. The mixture is refluxed for 5 hours and then concentrated under reduced pressure, and ice water is added to the residue. Extraction with dichloromethane, washing with saturated sodium chloride solution until neutral, clarification over anhydrous sodium sulphate and concentration gives 4.6 g of a crude product, which is chromatographed on 120 g of silica gel using toluene/petroleum ether (ratio 1:1). 1.2 g of 4-bromo-1-(2,4,6-trichloro-phenyl)-3-trifluoromethylpyrazole of melting point 93°-94° C. (from petroleum ether) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876393 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-e323f4fb137046658e9e11a4e3f5af54 |
| Source note | uspto-grants-1989_10 |