돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7829생성일: 2026년 10월 24일

Sodium Hydroxide → 9a-[(1E)-1-butenyl]-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/ko/reaction/7829

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-[(1E)-1-butenyl]-5-methoxy-2-(3-oxopentyl)-1-indanoneHCID 21990882—
용매MethanolHCID 887—
생성물9a-[(1E)-1-butenyl]-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 2199089935.8%

반응 조건

온도85 °C

반응 단계

A solution of 2-[(1E)-1-butenyl]-5-methoxy-2-(3-oxopentyl)-1-indanone (199 mg, 0.663 mmol) in methanol (5 mL) was treated with 2N aqueous NaOH (1.6 mL) and the resulting mixture was stirred and heated in an oil bath at 85° C. for 7 hours. After cooling to room temperature, the brown solution was partitioned between EtOAc (20 mL) and 0.4N HCl (10 mL). The organic phase was separated, washed with brine (15 ml), dried over MgSO4, filtered, and evaporated under vacuum to a brown oil (208 mg). The crude product was purified by silica gel chromatography on a Biotage FLASH 12S column (1.2×7.5 cm), eluting with 5:1 hexanes:EtOAc, to afford 9a-[(1E)-1-butenyl]-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (67 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0caa973e2b6a45ab9fd8c25a7a357edd
출처 메모uspto-grants-2006_08