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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11571생성일: 2026년 10월 24일

Acetamidomalonic acid diethyl ester → Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate

https://huagongshe.com/ko/reaction/11571

반응식

참여 물질

역할이름HCID투입량
반응물Acetamidomalonic acid diethyl esterHCID 14041—
반응물Benzene, 2-(bromomethyl)-1-methoxy-3-nitro-HCID 186047—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonateHCID 2197461580.8%

반응 단계

Sodium metal (1.15 g) was dissolved in absolute ethanol (500 mL), and to the resulting solution was added diethyl 2-acetylaminomalonate (9.1 g). After 15 min at room temperature, a solution of 2-methoxy-6-nitrobenzyl bromide (J. Med. Chem. 1977, 20, 190–196) (8.6 g) in tetrahydrofuran (25 mL) was added over 2 min. After 16 h stirring at room temperature the mixture was evaporated. The residue was dissolved in a mixture of ethyl acetate and water. The ethyl acetate layer was separated and washed sequentially with water and brine before drying over anhydrous sodium sulfate. Evaporation was followed by silica gel chromatography eluting initially with dichloromethane, followed by ethyl acetate, to obtain diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate (10.8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098235B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f049805b02c647ba9683e13a05b400db
출처 메모uspto-grants-2006_08