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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7821생성일: 2026년 10월 23일

Bromine → 4-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/ko/reaction/7821

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물Sodium BicarbonateHCID 516892—
반응물7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 21990903—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물4-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 2199086046.5%

반응 단계

A mixture of 7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (32 mg, 0.14 mmol) and NaHCO3 (60 mg, 0.7 mmol) in CH2Cl2 (0.5 ml) was treated with bromine (0.008 mL, 0.154 mmol), and the resulting mixture was stirred at room temperature for 22 hours. The mixture was diluted with EtOAc (8 ml), washed with dilute aqueous Na2S2O3 (4 mL) and brine (4 ml), dried over MgSO4, filtered, and evaporated under vacuum to a yellow oil (43 mg). This material was purified by preparative layer chromatography on a 0.05×20×20 cm silica gel GF plate, developing twice with CH2Cl2, to afford 4-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (20 mg) as a gum. The product was contaminated with a trace of 4,6-dibromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ca78e012a7fe470cbc127bc7a9674487
출처 메모uspto-grants-2006_08