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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Fluorophenylhydrazine hydrochloride | HCID 69981 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | (E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile | HCID 86680352 | — |
| 反応物 | (Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile | HCID 86680353 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846746B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-afc7bcc94e5c4b498feaeb05f2571b71 |
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| 出典メモ | uspto-grants-2014_09 |
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