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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15652생성일: 2026년 10월 23일

Tributylphosphine → methyl[(3S)-6-({2'-(acetoxymethyl)-6'-methyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetate

https://huagongshe.com/ko/reaction/15652

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(3'-(Hydroxymethyl)-6-methyl-4-[3-(methylsulfonyl)propoxy]biphenyl-2-yl)methyl acetateHCID 59342573—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
생성물methyl[(3S)-6-({2'-(acetoxymethyl)-6'-methyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetateHCID 5934259779%

반응 단계

A solution of methyl[(3S)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]acetate (0.208 g, 1.00 mmol), (3′-(hydroxymethyl)-6-methyl-4-[3-(methylsulfonyl)propoxy]biphenyl-2-yl)methyl acetate (0.360 g, 1.00 mmol) and tributylphosphine (0.324 g, 1.60 mmol) in toluene (15 mL) was stirred, 1,1′-(azodicarbonyl)dipiperidine (0.404 g, 1.60 mmol) was added, and the mixture was stirred at room temperature for 3 hr under nitrogen atmosphere. Hexane (8 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=30:70-70:30) to give the title compound (0.432 g, yield 79%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732626B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6a7924da036c476781bb9ebc7bbc46e5
출처 메모uspto-grants-2010_06