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HRID 273396생성일: 2026년 10월 26일

Triphenylphosphine → Methyl 3-(4-{[2'-methyl-4'-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoate

https://huagongshe.com/reaction/273396

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물PyripropanolHCID 72922—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Methyl 3-{4-[(4'-hydroxy-2'-methylbiphenyl-3-yl)methoxy]phenyl}propanoateHCID 58903183—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-(4-{[2'-methyl-4'-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoateHCID 5890313556.2%

반응 단계

A solution of methyl 3-{4-[(4′-hydroxy-2′-methylbiphenyl-3-yl)methoxy]phenyl}propanoate (0.602 g, 1.60 mmol), 3-(pyridin-2-yl)propan-1-ol (0.822 g, 6.00 mmol) and triphenylphosphine (1.57 g, 6.00 mmol) in tetrahydrofuran (20 mL) under ice-cooling was stirred and diethyl azodicarboxylate (40% toluene solution, 2.72 mL, 6.00 mmol) was added. The mixture was warmed to room temperature and stirred for 42 hrs. The reaction mixture was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (20%-60% ethyl acetate/hexane) and preparative HPLC to give the title compound as a yellow viscous oil (0.446 g, yield 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456218B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-15d8bc15785e4575bd3d9f7d1597243e
출처 메모uspto-grants-2008_11