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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39191생성일: 2026년 10월 24일

Diethyl methylmalonate → Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate

https://huagongshe.com/ko/reaction/39191

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl methylmalonateHCID 11857—
반응물Sodium hydrideHCID 24758—
반응물2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
용매DimethylformamideHCID 6228—
생성물Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonateHCID 5920613299%

반응 조건

온도0 °C

반응 단계

Diethyl 2-methylmalonate (4.31 mL, 25.0 mmol) was dissolved in 25 mL of anhydrous DMF. This solution was cooled to 0° C. under an atmosphere of nitrogen. Sodium hydride (1.04 g, 26 mmol, 60% by weight in mineral oil) was slowly added to the solution. The resulting mixture was allowed to stir for 3 minutes at 0° C., and then at room temperature for 10 minutes. 2-Bromo-1-fluoro-4-nitrobenzene (5.00 g, 22.7 mmol) was quickly added and the mixture turned bright red. After stirring for 10 minutes at room temperature, the crude mixture was evaporated to dryness and then partitioned between dichloromethane and a saturated aqueous solution of sodium chloride. The layers were separated and the organic phase was washed twice with a saturated aqueous solution of sodium chloride. The organics were concentrated to yield diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate (8.4 g, 99%) as a pale yellow oil which was used without further purification. Retention time 1.86 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524767B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-36d28dae0c694402b63d442f4eef0be0
출처 메모uspto-grants-2013_09