Reaktion #6171

Reaktionsgleichung

imidazole

chlorotriisopropylsilane

H2O

(3S,4S)-N-[(tertbutyloxy)carbonyl]-4-amino-3-hydroxy-5-phenyl pentene

→

title compound

Ausbeute 82.0%

(3S,4S)-N-[(tert-Butyloxy)-carbonyl]-4-amino-5-phenyl-3-(triisopropylsilyloxy)-pentene

Ausbeute 82.0%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionextracted with Et2O (2×25 mL)
2. 2
   WaschenThe combined organic layers were washed with H2O (250 mL)
3. 3
   TrocknenAfter the organic layer was dried over MgSO4
4. 4
   Einengenthe filtrate was concentrated
5. 5
   Sonstigepurified by medium pressure column chromatography (silica gel, 10% ethyl acetate in hexane, Rf 0.23)

Vorschrift

A solution of (3S,4S)-N-[(tertbutyloxy)carbonyl]-4-amino-3-hydroxy-5-phenyl pentene [prepared by the method of Hanson et al, J. Org. Chem., 50, 5399 (1985)] (10.0 g, 64.5 mmol), imidazole (9.14g, 13 mmol), and chlorotriisopropylsilane (12.44 g, 43.3 mmol) in anhydrous DMF (40 mL) was stirred for 5 days at room temperature under an N2 atmosphere. The solution was poured into H2O (500 mL) and extracted with Et2O (2×25 mL). The combined organic layers were washed with H2O (250 mL), a 0.5M citric acid solution (2×120 mL), a 5% KHCO3 solution (2×100 mL), and brine (2×100 mL). After the organic layer was dried over MgSO4, the filtrate was concentrated and purified by medium pressure column chromatography (silica gel, 10% ethyl acetate in hexane, Rf 0.23) to give 12.9 g (82 % yield) of the title compound as a clear, colorless oil. 1H and 13C NMR spectral data were consistent with the proposed structure.

Quelle