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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15640생성일: 2026년 10월 25일

Tributylphosphine → methyl[(3S)-6-({4'-[2-(ethylthio)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetate

https://huagongshe.com/reaction/15640

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물(S)-Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetateHCID 53393313—
반응물{4'-[2-(Ethylthio)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methanolHCID 59342614—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
생성물methyl[(3S)-6-({4'-[2-(ethylthio)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetateHCID 5934255760%

반응 단계

A solution of methyl[(3S)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]acetate (0.250 g, 1.20 mmol), {4′-[2-(ethylthio)ethoxy]-2′,6′-dimethylbiphenyl-3-yl}methanol (0.380 g, 1.20 mmol) and tributylphosphine (0.388 g, 1.92 mmol) in toluene (20 mL) was stirred, 1,1′-(azodicarbonyl)dipiperidine (0.484 g, 1.92 mmol) was added, and the mixture was stirred at room temperature for 1 hr under nitrogen atmosphere. Hexane (10 mL) was added to the reaction mixture, the precipitated insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-40:60) to give the title compound (0.363 g, yield 60%) as a pale-yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732626B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3b8d2eeac70e4f3b8da5bb99e838878e
출처 메모uspto-grants-2010_06