反应详情

To a solution of 1.26 g of 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl (2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl carbonate in 35 mL of CH2Cl2 cooled at −78° C. was added 1.05 g of Dess-Martin reagent. After 1 h of stirring at rt, the reaction was quenched with aqueous NaHCO3, extracted with EtOAc, washed with aqueous NaHCO3 and brine, dried over sodium sulfate, filtered through a pad of silica gel by eluting with EtOAc and evaporated. The crude material obtained was dissolved in a solvents mixture of 175 mL of t-BuOH and 75 mL of H2O, and treated with 6.07 g of NaH2PO4 mono hydrated and 6.07 g of NaClO2 for 30 min in the presence of 30 mL of 2-methyl-2-butene. The organic solvents were removed under vacuum. The crude material was diluted with EtOAc, washed with aqueous 1N HCl and brine, dried over Na2SO4, and evaporated. The crude acid obtained was diluted with THE and esterified with diazomethane (excess). The reaction mixture was concentrated and the residue was purified by flash chromatography (10–50% EtOAc/hexane) to afford 1.02 g of the title compound as a colorless oil.

1. customthe reaction was quenched with aqueous NaHCO3
2. extractionextracted with EtOAc
3. washwashed with aqueous NaHCO3 and brine
4. dry with materialdried over sodium sulfate
5. filtrationfiltered through a pad of silica gel
6. washby eluting with EtOAc
7. customevaporated
8. customThe crude material obtained
9. customThe organic solvents were removed under vacuum
10. additionThe crude material was diluted with EtOAc
11. washwashed with aqueous 1N HCl and brine
12. dry with materialdried over Na2SO4
13. customevaporated
14. customThe crude acid obtained
15. additionwas diluted with THE and
16. concentrationThe reaction mixture was concentrated
17. customthe residue was purified by flash chromatography (10–50% EtOAc/hexane)