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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2267607생성일: 2026년 10월 25일

Dimethylformamide → Dimethyl [2-(4-fluoro-2-nitrophenyl)-1-phenylethyl]malonate

https://huagongshe.com/reaction/2267607

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물4-Fluoro-2-nitrotolueneHCID 67965—
반응물2-Phenyl-1,3-dioxane-4,6-dioneHCID 933829—
반응물Ethyl acetate hexaneHCID 21226206—
생성물Dimethyl [2-(4-fluoro-2-nitrophenyl)-1-phenylethyl]malonateHCID 5968851430%

반응 단계

A solution of benzylidene malonate (14.2 g) in DMF (280 mL) was treated with sodium hydride (2.57 g, 95%). A solution of 4-fluoro-2-nitrotoluene in DMF (10 mL) was added over 1H, and the reaction mixture was stirred at RT overnight and then quenched by the addition of glacial acetic acid (175 mL) at 0° C. A total of 500 mL of 70:30 water-methanol was added with stirring, and the organics were extracted with ethyl acetate. The organic extracts were combined and washed with saturated aqueous potassium carbonate solution (2×) and brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give a dark brown oil. Flash chromatography on silica gel (75:25 hexane-ethyl acetate, then 50:50 hexane-ethyl acetate) provided 7.0 g (30%) of the title compound as a red-brown solid. 1H NMR (300 MHz, CDCl3) δ 3.72 (d, 2H), 3.73 (d, 1H), 4.32 (m, 1H), 7.09-7.29 (m, 7H), 7.71 (m, 1H). MS APCI, m/z=398 (M+Na). LC/MS: 2.66 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07858776B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-d1c05d2a8f4d47f5ba7021ba682c1f15
출처 메모uspto-grants-2010_12