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HRID 28614作成日:2026年10月24日

Methyl 4-nitrobenzoate → 1-(4-Nitrophenyl)-2,2,2-trifluoroethane-1,1-diol

https://huagongshe.com/ja/reaction/28614

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-nitrobenzoateHCID 12083—
反応物(Trifluoromethyl)trimethylsilaneHCID 552549—
反応物Tetrabutylammonium FluorideHCID 2724141—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Nitrophenyl)-2,2,2-trifluoroethane-1,1-diolHCID 6898756747%

反応条件

温度-78 °C

反応手順

To a mixture of 4-nitro-benzoic acid methyl ester (1.8 g, 9.9 mmol), trimethyl-trifluoromethyl-silane (2.0 ml, 12.8 mmol) and anhydrous dichloromethane (20 ml), cooled at −78° C., was added a solution of tetrabutylammonium fluoride in dichloromethane (1 M, 0.5 ml) previously dried over 4A molecular sieves. After stirring for 72 hours, hydrochloric acid (1 M, 50 ml) was added. The mixture was treated with saturated aqueous sodium chloride solution (100 ml) and extracted with ethyl acetate (100 ml). The organic extract was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:3) providing 2,2,2-trifluoro-1-(4-nitro-phenyl)-ethane-1,1-diol (1.1 g, 47% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-22b8025c6fed4512a99f7b5726576bc2
出典メモuspto-grants-2008_09