HRID1039727

反应详情

EQUATION

反应方程式

HRID 1039727 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of tert-butyl (1R,2S)-2,3-bis(tert-butyldimethylsilyloxy)-1-(thiazol-2-yl)propylcarbamate (6.150 g, 12.2 mmol) in 120 mL MeCN was treated with 4A mol. sieves and was allowed to stir at room temperature for 10 minutes. Methyl trifluoromethylsulfonate (1.62 ml, 14.7 mmol) was added, and the reaction mixture was allowed to stir for an additional 30 minutes. The reaction mixture was then concentrated in vacuo. The crude residue was dissolved in 100 mL MeOH, cooled to 0° C., and treated with NaBH4 (1.39 g, 36.7 mmol). The reaction mixture was allowed to warm to RT and stir for an additional 20 minutes. The reaction mixture was then concentrated, diluted with EtOAc, filtered through celite and again concentrated in vacuo. The residue was dissolved in 100 mL ACN and 20 mL water and was treated with mercury(II)chloride (3.32 g, 12.2 mmol). After stirring for 30 minutes, an additional portion of NaBH4 (1.39 g, 36.7 mmol) was added, and the reaction mixture was allowed to stir for another 30 minutes. The reaction mixture was quenched with saturated NaHCO3 solution and diluted with EtOAc. The crude reaction mixture was then washed with water then brine. The organic layer was dried over MgSO4 and concentrated in vacuo. The crude residue was forced through a short plug of silica eluting with ether. The filtrate was again concentrated in vacuo yielding tert-butyl (2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-hydroxybutan-2-ylcarbamate (5.33 g, 96.9% yield) with minor impurities.

WORKUP

后处理

  1. stirringto stir for an additional 30 minutes
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. dissolutionThe crude residue was dissolved in 100 mL MeOH
  4. temperaturecooled to 0° C.
  5. temperatureto warm to RT
  6. stirringstir for an additional 20 minutes
  7. concentrationThe reaction mixture was then concentrated
  8. additiondiluted with EtOAc
  9. filtrationfiltered through celite
  10. concentrationagain concentrated in vacuo
  11. dissolutionThe residue was dissolved in 100 mL ACN
  12. stirringAfter stirring for 30 minutes
  13. stirringto stir for another 30 minutes
  14. customThe reaction mixture was quenched with saturated NaHCO3 solution
  15. additiondiluted with EtOAc
  16. customThe crude reaction mixture
  17. washwas then washed with water
  18. dry with materialThe organic layer was dried over MgSO4
  19. concentrationconcentrated in vacuo
  20. concentrationThe filtrate was again concentrated in vacuo