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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8476생성일: 2026년 10월 23일

Water → (S)-Diethyl (7,8-Difluoro-3-Methyl-3,4-Dihydro-2H-[1,4]Benzoxazin-4-Yl)Methylene-Malonate

https://huagongshe.com/ko/reaction/8476

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diethyl (ethoxymethylene)malonateHCID 6871—
반응물Potassium HydroxideHCID 14797—
반응물Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonateHCID 11485652—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매DimethylformamideHCID 6228—
생성물(S)-Diethyl (7,8-Difluoro-3-Methyl-3,4-Dihydro-2H-[1,4]Benzoxazin-4-Yl)Methylene-MalonateHCID 11089557—

반응 조건

온도60 °C

반응 단계

Potassium hydroxide (180 mg) and tetrabutylammonium hydrogensulfate (90.4 mg) were dissolved in DMF (15 ml) by heating to 60° C. and a solution of diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonate (1g, 99.8% ee) and diethyl ethoxymethylenemalonate (120 mg) in DMF 85 ml) was added thereto. The obtained mixture was stirred at the same temperature for 2 hours. After adding water, the liquid reaction mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography. Thus, 852 mg (99.8% ee) of the title compound was obtained as a yellow oily substance. Various spectral data was identical with those described in Japanese Patent No. 2,769,174.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087778B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7714985961f941faaa20baf817e41c9a
출처 메모uspto-grants-2006_08