反应详情

To (2R,3S)-3-(tert-butyl-dimethylsilanyloxy)-2-hydroxymethyl pyrrolidine-1-carboxylic acid tert-butyl ester (61A) (9.85 g, 29.7 mmol) in CH2Cl2 (200 mL) at 0° C. was added Dess-Martin periodinane. The ice bath was removed and the reaction was warmed to rt. After 2 h, saturated aqueous Na2S2O3 and NaHCO3 (ca. 100 mL each) were added and the reaction mixture was stirred vigorously for 0.5 h. The layers were separated, and the organic layer was washed with a mixture of saturated aqueous Na2S2O3 and saturated aqueous NaHCO3 followed by brine, dried (MgSO4), and was then filtered and concentrated to obtain the title compound (9.23 g) as a yellow oil.

1. customThe ice bath was removed
2. additionsaturated aqueous Na2S2O3 and NaHCO3 (ca. 100 mL each) were added
3. customThe layers were separated
4. washthe organic layer was washed with a mixture of saturated aqueous Na2S2O3 and saturated aqueous NaHCO3
5. dry with materialdried (MgSO4)
6. filtrationwas then filtered
7. concentrationconcentrated