反应详情

To a solution of (R)-tert-butyl 3-(N-methoxy-N-methylcarbamoyl)piperidine-1-carboxylate (0.65 g, 2.37 mmol) in THF (4 mL) at −20° C. was added dropwise the solution of 2-(3-fluorophenoxy)phenyllithium prepared in Step 2 above. After the addition was complete, the resulting solution was allowed to warm to rt slowly, and left at rt for 1 h. The reaction was quenched with 1N HCl (˜6 mL), and extracted with Et2O (4×10 mL). The combined organic layers were washed with sat'd aq NaHCO3 and brine, and dried over Na2SO4. Removal of the solvent left the crude ketone (1.49 g, quantitative), which was used for next step without further purification.

1. additionAfter the addition
2. customThe reaction was quenched with 1N HCl (˜6 mL)
3. extractionextracted with Et2O (4×10 mL)
4. washThe combined organic layers were washed with sat'd aq NaHCO3 and brine
5. dry with materialdried over Na2SO4
6. customRemoval of the solvent
7. waitleft the crude ketone (1.49 g, quantitative), which
8. customwas used for next step without further purification