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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5344생성일: 2026년 10월 23일

Water → 2-Oxo-3-carboethoxy-4-(2-bromo-5-methoxyphenyl)butanoic acid, ethyl ester

https://huagongshe.com/ko/reaction/5344

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diethyl EtherHCID 3283—
반응물Diethyl OxalateHCID 7268—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-Bromo-5-methoxyphenyl-propionateHCID 131718119—
생성물2-Oxo-3-carboethoxy-4-(2-bromo-5-methoxyphenyl)butanoic acid, ethyl esterHCID 1566234090%

반응 조건

온도0 °C

반응 단계

Potassium t-butoxide (6.72 g) was suspended in 30 ml of anhydrous ether and cooled to 0° C. A solution of 14.35 g of ethyl 3-(2-bromo-5-methoxyphenyl-propionate and 10.95 g diethyl oxalate in 10 ml ether was added dropwise over 15 min. After 2 at 25° C., the reaction was poured into 100 ml H2O and the aqueous layer was separated, acidified to pH 1 and extracted with ether. The ether layer was dried (MgSO4) and the solvent was evaporated to yield 17.48 g of the desired product as a colorless oil (90%). NMR (CDCl3) δ1.20 (t, 3H), 1.35 (t, 3H), 3.32 (dd, 2H), 3.76 (s, 3H), 4.18 (q, 2H), 4.32 (q, 2H), 4.53 (t, 1H), 6.67 (dd, 1H), 6.80 (d, 1H), 7.40 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244888
출처 데이터셋uspto-grants-1993_09
ORD IDord-29b1539b5e8e4303be8267bfa4999d0d
출처 메모uspto-grants-1993_09