HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843020Generated: November 3, 2026
Hydrazine, dihydrochloride → 3-(Trifluoromethyl)pyrazole
https://huagongshe.com/reaction/1843020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine, dihydrochloride | HCID 17548 | — |
| Reactant | (3E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one | HCID 5709222 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Trifluoromethyl)pyrazole | HCID 1807034 | — |
Reaction Steps
Hydrazine dihydrochloride (225 g, 2.14 mol) in ethanol (1400 mL) was stirred well. TEA (185.4 mL, 1.34 mol) was added drop wise for 45 min at ambient temperature. Then (E)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one (225 g, crude) was added drop wise at room temperature and the overall reaction mixture was refluxed overnight. Progress of the reaction was monitored by TLC (20% ethyl acetate/hexane, Rf˜0.4). On completion of the reaction, ethanol was distilled off completely, residue was taken in ice water (500 mL) and the product extracted with ethyl acetate (2×400 mL). Combined extract was washed with ice water (300 mL), dried over sodium sulfate and concentrated under reduced pressure to yield 3-(trifluoromethyl)-1H-pyrazole as a off white solid (175 g, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946204B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-39c58c780c7c49e0bbd205b45820b6aa |
|---|
| Source note | uspto-grants-2015_02 |
|---|