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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7856생성일: 2026년 10월 24일

2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone → 9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/ko/reaction/7856

반응식

참여 물질

역할이름HCID투입량
반응물2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanoneHCID 21990911—
용매Acetic AcidHCID 176—
용매Hydrochloric AcidHCID 313—
용매Ethyl AcetateHCID 8857—
생성물9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 2199087660.6%

반응 조건

온도90 °C

반응 단계

A solution of 2-butyl-4-chloro-5-methoxy-2-(3-oxo-pentyl)-1-indanone (250 mg, 0.74 mmol) in acetic acid (2 mL) was diluted with 6N aqueous HCl (2 mL). The resulting mixture was stirred and heated in an oil bath at 90° C. for 18 hours, then kept at room temperature for 2 days. The mixture was diluted with EtOAc (20 mL), washed with water (30 mL), 5% NaHCO3 (10 mL) and brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (250 mg). The crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates, developing with 5% EtOAc in CH2Cl2, to afford 9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (143 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6121252028114c99b582eb81c90945f8
출처 메모uspto-grants-2006_08