HRID515502

反应详情

EQUATION

反应方程式

HRID 515502 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

(R)-(2-Hydroxy-1-methyl-ethyl)-carbamic acid tert-butyl ester (4.0 g, 22.8 mmol) was dissolved in 50% aqueous sodium hydroxide solution (15 mL) at 0° C. and to the resulting solution was added allylbromide (2.2 mL, 25 mmol) and catalytic amount of tetrabutylammonium hydrogensulfate (0.85 g, 2.5 mmol) at room temperature and stirred for 4 hours. The resulting solution was diluted with water and extracted with ethyl acetate. The organic extracts were dried over anhydrous sodium sulfate and concentrated. The resulting crude allyl ether was dissolved in THF (75 mL) at room temperature and to the resulting solution was added a solution of 9-borabicyclo[3,3,1]nonane in THF (0.5 M, 100 mL, 50 mmol). After 5 hour-stirring, to the resulting solution was added water (8 mL), 3N aqueous sodium hydroxide solution (8.1 mL) and 30% aqueous hydrogen peroxide solution (8.2 mL) at room temperature and warmed to 40° C. followed by stirring for 30 minutes. The organic solvent was removed under reduced pressure and the residue was diluted with brine. Extraction was performed with ethyl acetate and the extracts were dried over magnesium sulfate. After concentration, the residual materials were purified by flash column chromatography on silica gel to afford (R)-[2-(3-hydroxypropoxy)-1-methyl-ethyl]carbamic acid tert-butyl ester (3.0 g, 12.9 mmol, 56%) as a colorless oil.

WORKUP

后处理

  1. extractionextracted with ethyl acetate
  2. dry with materialThe organic extracts were dried over anhydrous sodium sulfate
  3. concentrationconcentrated
  4. dissolutionThe resulting crude allyl ether was dissolved in THF (75 mL) at room temperature and to the resulting solution
  5. stirringAfter 5 hour-stirring, to the resulting solution
  6. stirringby stirring for 30 minutes
  7. customThe organic solvent was removed under reduced pressure
  8. additionthe residue was diluted with brine
  9. extractionExtraction
  10. dry with materialthe extracts were dried over magnesium sulfate
  11. concentrationAfter concentration
  12. customthe residual materials were purified by flash column chromatography on silica gel