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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

反応式

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-butanedioneHCID 67594—
反応物2-Chlorophenylhydrazine hydrochlorideHCID 443287—
溶媒Acetic AcidHCID 176—
生成物1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazoleHCID 57458236—

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07998995B2
出典データセットuspto-grants-2011_08
ORD IDord-366052737cb44f529b6cfae74b4e0fa8
出典メモuspto-grants-2011_08