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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8474생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/8474

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diethyl (ethoxymethylene)malonateHCID 6871—
반응물Potassium HydroxideHCID 14797—
반응물(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매DimethylformamideHCID 6228—
생성물Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonateHCID 1148565290.2%

반응 조건

온도0 °C

반응 단계

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 (1.65 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087778B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b70b5d96668a4a3a90823c7b62b9d362
출처 메모uspto-grants-2006_08