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HRID 259788생성일: 2026년 10월 26일

Triphenylphosphine → Methyl 3-((2-(N-t-Butyloxycarbonyl-N-methylamino)ethoxy))benzoate

https://huagongshe.com/reaction/259788

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Methyl 3-HydroxybenzoateHCID 88068—
반응물N-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-((2-(N-t-Butyloxycarbonyl-N-methylamino)ethoxy))benzoateHCID 1893072972.3%

반응 단계

Methyl 3-hydroxybenzoate (6.4 g, 42 mmol), alcohol 121a (7.4 g, 42 mmol), diisopropyl azodicarboxylate (8.3 mL, 42 mmol), and triphenylphosphine (11.1 g, 42 mmol) were stirred in dry THF (120 mL) at 0 ° C. for 1 h, then for 18 h at room temperature. After evaporation of solvent, the product was isolated by chromatography on silica gel, eluting with 0% to 30% EtOAc in hexane to yield a clear oil (9.4 g). IR(film) cm-1 1726, 1696. 1H NMR(300 MHz, CDCl3): 7.64-7.09 (m, 4H), 4.13 (m, 2H), 3.92 (s, 3H), 3.62 (br, 2H), 2.99 (s, 3H), 1.46 (s, 9H). Anal. Cald'd for C16H23NO5 : C, 62.11; H, 7.51; N, 4.53; Found: C, 61.67; H, 7.43; N, 4.47. HR-MS: Calc'd. 310.1654, Found 310.1650.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05523302
출처 데이터셋uspto-grants-1996_06
ORD IDord-92de8bfaa49944c8b84e9082495015b5
출처 메모uspto-grants-1996_06