HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871516Generated: October 30, 2026
Phenylhydrazine hydrochloride → 1-phenyl-3-(trifluoromethyl)-1H-pyrazol-5-amine
https://huagongshe.com/reaction/871516
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Reactant | 4,4,4-Trifluoro-3-oxobutanenitrile | HCID 13843540 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-phenyl-3-(trifluoromethyl)-1H-pyrazol-5-amine | HCID 43158951 | 91% |
Reaction Steps
A mixture of 4,4,4-trifluoro-3-oxobutanenitrile (2.056 g, 15 mmol) and phenylhydrazine hydrochloride (2.169 g, 15 mmol) in EtOH was heated at 90° C. for 8 hours. The reaction was quenched with water, basified with saturated NaHCO3 solution, and extracted with CH2Cl2. Extracts were dried over MgSO4, concentrated under reduced pressure, and dried under vacuum to afford 1-phenyl-3-(trifluoromethyl)-1H-pyrazol-5-amine as yellow solid (3.089 g, 91%). 1H NMR (300 MHz, CDCl3) δ 7.54 (m, 5H), 5.85 (s, 1H), 3.95 (br, 2H); LC-MS (ESI) m/z 228 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969587B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6e46e8f323814271aad5712cfef73a22 |
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| Source note | uspto-grants-2015_03 |
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