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HRID 83493作成日:2026年10月26日

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

https://huagongshe.com/reaction/83493

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorophenylhydrazine hydrochlorideHCID 69981—
反応物Sodium ethoxideHCID 2723922—
反応物(E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrileHCID 86680352—
反応物(Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrileHCID 86680353—
溶媒EthanolHCID 702—
生成物1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamineHCID 71287743—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846746B2
出典データセットuspto-grants-2014_09
ORD IDord-afc7bcc94e5c4b498feaeb05f2571b71
出典メモuspto-grants-2014_09