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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4462생성일: 2026년 10월 23일

Acetic Acid → 4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-penten-1-ol

https://huagongshe.com/ko/reaction/4462

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Diethyl EtherHCID 3283—
반응물Diisobutylaluminum hydrideHCID 14487—
반응물4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-pentenoic acid, methyl esterHCID 86741998—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-penten-1-olHCID 5437276774%

반응 조건

온도-78 °C

반응 단계

To a solution of 4.5 g (10.6 mmol) 4-(4-(4-bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-pentenoic acid, methyl ester in 25 ml toluene at -78° C. was added dropwise over a period of 30 min, 16.5 ml of 1.5M DIBAL-H in toluene, keeping the temperature below -60° C. The mixture was stirred for 21/2 hours at -78° C. To the mixture was added 17 ml of a 75:25:6 ether:acetic acid:water mixture, keeping the temperature below -60° C. The mixture was then allowed to warm to room temperature and the solid material was filtered off. The filtrate was washed twice with saturated NaHCO3 and once with water, dried over MgSO4 and the solvent was removed by rotary evaporation. The residue was purified by HPLC, eluting with 80:20 hexane:acetone, to give 3.1 g (74%) of the product as a pale yellow oil which was used immediately in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725683
출처 데이터셋uspto-grants-1988_02
ORD IDord-06486a43573049c0972d0737d58446eb
출처 메모uspto-grants-1988_02