Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237448생성일: 2026년 10월 25일
Tributylphosphine → Methyl 2-((S)-6-((R)-4-(2,6-dimethyl-4-(2-(methylthio)ethoxy)phenyl)-7-fluoro-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate
https://huagongshe.com/reaction/237448
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 반응물 | 2-(Methylthio)ethanol | HCID 78925 | — |
| 반응물 | Methyl 2-((S)-6-((R)-7-fluoro-4-(4-hydroxy-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate | HCID 86697113 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Methyl 2-((S)-6-((R)-4-(2,6-dimethyl-4-(2-(methylthio)ethoxy)phenyl)-7-fluoro-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate | HCID 86697114 | — |
반응 단계
To a solution of methyl 2-((S)-6-((R)-7-fluoro-4-(4-hydroxy-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate (280 mg) and 2-(methylthio)-ethanol (54 μL) in toluene (8 mL) are successively added 1,1′-(azodicarbonyl)-dipiperidine (240 mg) and tributylphosphine (240 mL). The mixture is stirred for 12 hours at room temperature, partitioned between saturated aqueous NaHCO3 solution and dichloromethane and stirred for 30 minutes. The phases are separated and the organic phase is dried (MgSO4). The solvents are evaporated and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 90:10→70:30) to give the title compound. Yield: 235 mg; LC (method 4): tR=1.97 min; Mass spectrum (ESI+): m/z=537 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642585B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-2fdc42aaa62e49c4826c7d38d06c9a01 |
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| 출처 메모 | uspto-grants-2014_02 |
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