HRID221541

反应详情

EQUATION

反应方程式

HRID 221541 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

(2R)-2-amino-3-methylbutane-1,3-diol hydrochloride (4.32 g, 27.8 mmol) was dissolved in 10 mL of pyridine and the solution was stirred under N2. tert-Butyldimethylsilyl chloride (16.8 g, 111 mmol) and DMAP (339 mg, 2.8 mmol) were then added and the reaction mixture was heated to 65° C. After 3 days, the reaction was cooled and treated with in 3.5% NaH2PO4 solution. The solution was extracted with 200 mL CH2Cl2 and then with an additional 50 mL of CH2Cl2. The combined organic layers were washed with H2O and brine. The organic layer was then dried over Na2SO4, filtered and concentrate under reduced pressure. Chromatography (SiO2, 3% MeOH/CHCl3 with 0.1% NH4OH) gave (1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylpropylamine (5.85 g) as a light amber oil.

WORKUP

后处理

  1. temperaturethe reaction was cooled
  2. extractionThe solution was extracted with 200 mL CH2Cl2
  3. washThe combined organic layers were washed with H2O and brine
  4. dry with materialThe organic layer was then dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrate under reduced pressure