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HRID 30704作成日:2026年10月25日

Ammonium Chloride → HCID 86602516、化合物

https://huagongshe.com/reaction/30704

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物18-Crown-6HCID 28557—
反応物Nsc 634137HCID 184894—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23157484—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 86602516HCID 8660251695%

反応手順

Potassium bis(trimethylsilyl)amide (20% toluene solution, 3.05 g) was added to a mixture of bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate (973 mg), 18-crown-6 (4.04 g) and tetrahydrofuran (50 mL) at −78° C. Furthermore, 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (312 mg) was added and the mixture was stirred overnight while allowing to warm from −78° C. to room temperature. Saturated aqueous ammonium chloride was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with 1N hydrochloric acid, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to give methyl (2Z)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylate as crystals (0.35 g, yield 95%) from a fraction eluted with hexane-ethyl acetate (4:1-1:1, v/v) (recrystallized from ethyl acetate-hexane). melting point: 108-109° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-c8b7e21fd74f477c8b910c5ce184dcd9
出典メモuspto-grants-2008_09