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HRID 1672983作成日:2026年10月25日
4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione → 1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole
https://huagongshe.com/reaction/1672983
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione | HCID 67594 | — |
| 反応物 | 2-Chlorophenylhydrazine hydrochloride | HCID 443287 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole | HCID 57458236 | — |
反応手順
Into a 500 mL flask was weighed 25.0 g (139.6 mmol) of 2-chlorophenylhydrazine hydrochloride, 27.4 g (153 mmol) of 4,4,4-trifluoro-1-furan-2-yl-butane-1,3-dione, and 200 mL of acetic acid. The resulting solution was heated at 80° C. for 18 h then was cooled and was washed into a separatory funnel with 1.0 M NaOH and ethyl acetate. The ethyl acetate was separated, washed with 1.0 M NaOH, brine, dried (Na2SO4), and was concentrated in vacuo. The residue was filtered through a short column of silica gel affording 1-(2-chlorophenyl)-5-furan-2-yl-3-trifluoromethyl-1H-pyrazole as a brown oil, yield: 37.31 g (85%); MS (ES): 313 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07998995B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-366052737cb44f529b6cfae74b4e0fa8 |
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| 出典メモ | uspto-grants-2011_08 |
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