反应详情

1-(4-(Triisopropylsilyloxy)phenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanone (International Application Publication Number: WO 90/14088, Example 36 at page 41; 22.0 g, 45.7 mmol) was dissolved in dry tetrahydrofuran (500 mL). Tetrabutylammonium fluoride (55 ml, 55 mmol, 1N in tetrahydrofuran) was added dropwise to the stirred solution over 3 minutes. After stirring for 1 hour, the reaction mixture was concentrated and the concentrate flash chromatographed on silica gel (3×6 inches). The column was gradiently eluted with ethyl acetate/hexane, then sequentially with 100% ethyl acetate, 1:9 methanol:ethyl acetate and finally with 1:5 methanol: ethyl acetate. Product-containing fractions were stripped to yield 16.7 g (100%) of title product as a light yellow solid which was triturated with hexane; m.p. 95°-97° C.; 1H-NMR (CDCl3) delta (ppm) 8.08 (d, J=8.5 Hz, 2 H), 7.48 (d, J=8 Hz, 2 H), 7.34 (t, J=8 Hz, 2 H), 7.28-7.25 (m, 1 H partially obscured by CHCl3 from NMR solvent), 6.89 (d, J=8.5 Hz, 2 H), 4.15 (q, J=7 Hz, 1 H), 3.0-2.65 (m, 4 H), 2.25-2.10 (m, 2 H), 1.85-1.77 (m, 2 H), 1.35 (d, J=7 Hz, 3 H).

1. concentrationthe reaction mixture was concentrated
2. customthe concentrate flash chromatographed on silica gel (3×6 inches)
3. washThe column was gradiently eluted with ethyl acetate/hexane