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HRID 259788Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/259788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
EduktMethyl 3-HydroxybenzoateHCID 88068—
EduktN-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-((2-(N-t-Butyloxycarbonyl-N-methylamino)ethoxy))benzoateHCID 1893072972,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05523302
Quelldatensatzuspto-grants-1996_06
ORD IDord-92de8bfaa49944c8b84e9082495015b5
Quellennotizuspto-grants-1996_06