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HRID 8473作成日:2026年10月23日

Water → Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonate

https://huagongshe.com/ja/reaction/8473

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl (ethoxymethylene)malonateHCID 6871—
反応物Potassium HydroxideHCID 14797—
反応物(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒DimethylformamideHCID 6228—
生成物Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonateHCID 1148565292.9%

反応条件

温度0 °C

反応手順

At room temperature, potassium hydroxide (330 mg) and tetrabutylammonium hydrogensulfate (82.7 mg) were dissolved in DMF (15 ml). After adding a solution (5 ml) of (2S)-2-(2,3,4-trifluoroanilino)propanol (1 g, 99.8% ee) and diethylethoxymethylenemalonate (2.09 g) in DMF, the resultant mixture was stirred for 1 hour. After adding water, the liquid reaction mixture was extracted with a solvent mixture of ethyl acetate and n-hexane (3:2). The organic layer was washed with water and dried over anhydrous magnesium sulfate. After evaporating the solvent, IPE was added to the obtained residue and the mixture was stirred at 0° C. for 1 hour. The crystals thus precipitated were collected by filtration and the moist product thus obtained was dried under reduced pressure. Thus, the title compound (1.7 g, 99.8% ee) was obtained as colorless crystals. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 63.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087778B2
出典データセットuspto-grants-2006_08
ORD IDord-f4daeda6e673429492ae870b3e630a02
出典メモuspto-grants-2006_08