Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7838생성일: 2026년 10월 24일
Stannane, tributyl[4-(methoxymethoxy)phenyl]- → 9a-butyl-7-methoxy-4-(4-methoxymethoxy-phenyl)-1,2,9,9a-tetrahydro-3H-fluoren-3-one
https://huagongshe.com/ko/reaction/7838
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Stannane, tributyl[4-(methoxymethoxy)phenyl]- | HCID 10812390 | — |
| 반응물 | 4-bromo-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 21990931 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 9a-butyl-7-methoxy-4-(4-methoxymethoxy-phenyl)-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 21990890 | 84.5% |
반응 단계
A mixture of 4-bromo-9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (800 mg, 2.29 mmol), Pd(PPh3)4 (132 mg, 0.114 mmol), and tributyl-(4-methoxymethoxy-phenyl)-stannane (1.174 g, 2.75 mmol) in anhydrous toluene (11.5 mL) was placed under a nitrogen atmosphere and heated with stirring in an oil bath at 100° C. After 22 hours, the mixture was cooled to room temperature and evaporated under vacuum to a dark oil (2.208 g). This material was purified by chromatography on EM silica gel 60 (230-400 mesh, 115 mL dry), using 4:1 hexanes-EtOAc as eluting solvent, to afford 9a-butyl-7-methoxy-4-(4-methoxymethoxy-phenyl)-1,2,9,9a-tetrahydro-3H-fluoren-3-one (787 mg) as a yellow gum.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07087599B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-3dd93824a4984141a072324890d98328 |
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| 출처 메모 | uspto-grants-2006_08 |
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