HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83493Generated: October 25, 2026
4-Fluorophenylhydrazine hydrochloride → 1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine
https://huagongshe.com/reaction/83493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenylhydrazine hydrochloride | HCID 69981 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | (E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile | HCID 86680352 | — |
| Reactant | (Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile | HCID 86680353 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine | HCID 71287743 | — |
Reaction Steps
To a solution of a mixture of (E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile and (Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile (1.28 g) in ethanol (13 ml) were sequentially added 4-fluorophenylhydrazine hydrochloride (979 mg) and sodium ethoxide (20 wt % in ethanol, 5.0 ml), and the mixture was stirred overnight at reflux. This reaction solution was concentrated under reduced pressure, and then water was added thereto, and the mixture was extracted with ethyl acetate. This organic layer was sequentially washed with water and a saturated aqueous solution of sodium chloride, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1 to 1/1) to give the titled compound (1.29 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846746B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-afc7bcc94e5c4b498feaeb05f2571b71 |
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| Source note | uspto-grants-2014_09 |
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