Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7882생성일: 2026년 10월 23일
Stannane, tributyl(1-ethoxyethenyl)- → 9a-butyl-8-chloro-4-(1-ethoxyvinyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
https://huagongshe.com/ko/reaction/7882
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| 반응물 | 4-bromo-9a-butyl-8-chloro-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 21990872 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 9a-butyl-8-chloro-4-(1-ethoxyvinyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 21990909 | 76% |
반응 단계
A solution of 4-bromo-9a-butyl-8-chloro-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (90 mg, 0.235 mmol) in anhydrous toluene (1.2 mL) was treated with tributyl(1-ethoxyvinyl)stannane (0.111 mL, 0.352 mmol) and bis(triphenylphosphine)palladium(II) chloride (33 mg, 0.047 mmol). The mixture was placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 100° C. for 3 hours. After cooling to room temperature, the mixture was purified by preparative layer chromatography on two 0.1×20×20 cm silica gel GF plates, developing with 5% EtOAc in CH2Cl2. The product band was eluted with EtOAc and the eluent evaporated under vacuum to afford 9a-butyl-8-chloro-4-(1-ethoxyvinyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (67 mg) as an oil.
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-6e31e21fba51466aaf8cfe2488e576b3 |
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| 출처 메모 | uspto-grants-2006_08 |
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