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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 83493Erstellt: 24. Oktober 2026

4-Fluorophenylhydrazine hydrochloride → 1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine

https://huagongshe.com/de/reaction/83493

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluorophenylhydrazine hydrochlorideHCID 69981—
EduktSodium ethoxideHCID 2723922—
Edukt(E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrileHCID 86680352—
Edukt(Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrileHCID 86680353—
LösungsmittelEthanolHCID 702—
Produkt1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamineHCID 71287743—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846746B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-afc7bcc94e5c4b498feaeb05f2571b71
Quellennotizuspto-grants-2014_09