돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33946생성일: 2026년 10월 24일

Water → 2-Methoxy-5-(3,4,5-trimethoxyphenyl)-6,7,8,9-tetrahydro-benzocyclohepten-5-ol

https://huagongshe.com/ko/reaction/33946

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-Bromo-1,2,3-trimethoxybenzeneHCID 75885—
반응물2-Methoxy-6,7,8,9-tetrahydro-benzocyclohepten-5-oneHCID 266815—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물2-Methoxy-5-(3,4,5-trimethoxyphenyl)-6,7,8,9-tetrahydro-benzocyclohepten-5-olHCID 6892331149.6%

반응 조건

온도-30 °C

반응 단계

200 mL of anhydrous ether was, added to 3,4,5-trimethoxybromobenzene (1.23 g, 4.97 mmol) in a 500 mL round bottom flask under nitrogen. The temperature of the reaction mixture was brought to −78° C. n-Butyllithium (4.5 mL, 11.25 mmol) was added dropwise. The reaction mixture was then stirred until the temperature was raised gradually to −30° C. 30 (0.86 g, 4.5 mmol) dissolved in 25 mL of dry ether was added dropwise and the reaction mixture was allowed to stir until the temperature warmed up to room temperature. 25 mL of water was added and the product was extracted with ether (3×50), combined organic phases were dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. Purification by column chromatography (silica gel, 20:80 EtOAc:Hexanes) yielded 800 mg (49%) of 32 as pale yellow oil Rf: 0.16 (30:70, EtOAc:Hexanes).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429681B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f569a7b8886a4bcea5c27723d368f13a
출처 메모uspto-grants-2008_09