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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7836생성일: 2026년 10월 24일

4-bromo-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one → 4-Benzyl-9a-butyl-7-methoxy-1,2,9,9a-tetrahydrofluoren-3-one

https://huagongshe.com/ko/reaction/7836

반응식

참여 물질

역할이름HCID투입량
반응물4-bromo-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 21990931—
반응물5-Benzyl-1-aza-5-stanna-bicyclo[3.3.3]undecaneHCID 21990932—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물4-Benzyl-9a-butyl-7-methoxy-1,2,9,9a-tetrahydrofluoren-3-oneHCID 2199090595%

반응 조건

온도100 °C

반응 단계

A mixture of 4-bromo-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (29.6 mg, 0.0847 mmol), 5-benzyl-1-aza-5-stanna-bicyclo[3.3.3]undecane (38.5 mg, 85% weight pure, 0.0935 mmol), and Pd(PPh3)4 (9.8 mg, 0.00848 mmol) in anhydrous toluene (1.3 mL) was degassed, placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 100° C. After heating 4 hours, the cloudy, dark brown reaction mixture was cooled in an ice bath and filtered through a pad of celite. The filtrate was evaporated under vacuum to an orange gum (57 mg). The crude product was purified by preparative layer chromatography on a 0.1×20×20 cm silica gel GF plate, using 9:1 hexanes-EtOAc as developing solvent. The major UV visible band at Rf 0.18-0.26 was removed and eluted with EtOAc to afford 4-benzyl-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (29 mg) as a pale yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-38f635a0ee364faa8595c22f5d4de8f8
출처 메모uspto-grants-2006_08