反应详情

温度

0 °C

To a solution of (S)-tert-butyl 4-((R)-5-tert-butoxy-5-oxo-2-(tosyloxymethyl)pentyl)-2,2-dimethyloxazolidine-3-carboxylate (317 mg, 0.58 mmol) in anhydrous DCM (8 mL) at −78° C. under N2 was added DiBAlH (1 M in hexane, 1.75 mL, 1.75 mmol) dropwise. After the addition, the reaction mixture was stirred for another 30 min. The reaction was quenched with MeOH (2 mL), followed by 50% Rochelle's salt aq solution and stirred 2 hr. The resulting solution was extracted with DCM (3×20 mL), the combined organic phases were concentrated and dissolved in THF/MeOH (10 mL, 4/1, v/v), and chilled to 0° C., NaBH4 (11 mg, 0.29 mmol) was added and stirred at this temperature for 30 min. The reaction was quenched by aqueous NH4Cl, then extracted with EtOAc (3×20 mL), the combined organic phases were washed with H2O, brine, and dried over Na2SO4, and filtered, and concentrated to give crude product (S)-tert-butyl 4-((R)-5-hydroxy-2-(tosyloxymethyl)pentyl)-2,2-dimethyloxazolidine-3-carboxylate (255 mg, 92%). It was used without further purification.

1. additionAfter the addition
2. customThe reaction was quenched with MeOH (2 mL)
3. stirringstirred 2 hr
4. extractionThe resulting solution was extracted with DCM (3×20 mL)
5. concentrationthe combined organic phases were concentrated
6. dissolutiondissolved in THF/MeOH (10 mL, 4/1
7. stirringstirred at this temperature for 30 min
8. customThe reaction was quenched by aqueous NH4Cl
9. extractionextracted with EtOAc (3×20 mL)
10. washthe combined organic phases were washed with H2O, brine
11. dry with materialdried over Na2SO4
12. filtrationfiltered
13. concentrationconcentrated