HRID251518

反应详情

EQUATION

反应方程式

HRID 251518 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

To a solution of 2,3-dimethyl butene (300 ml, 2.42 mol) in 7.8 L of dry acetonitrile was added Chloramine-T (749.9 g, 1.1 eq) portionwise over 90 min. The temperature was maintained at approximately 20° C. To this reaction mixture was added phenyltrimethylammonium tribromide (91.4 g, 0.1 eq) in 10 g portions over 90 min. The temperature increased to 26° C. during the addition. The reaction mixture was stirred at room temperature for 2 days. The reaction mixture was concentrated down to approximately 15% of the initial volume and was them filtered, washing the solid with 1 L of acetonitrile. The organic liquid phase was concentrated and the residue dissolved in 2.5 L of EtOAc. The resulting solution was washed twice with water, dried over MgSO4, and concentrated to give a solid. The crude was purified on a large plug of celite using gradient elution 5% to 25% EtOAc/heptanes to afford 317 g of 2-isopropyl-2-methyl-1-[(4-methylphenyl)sulfonyl]aziridine as a solid.

WORKUP

后处理

  1. temperatureThe temperature increased to 26° C. during the addition
  2. concentrationThe reaction mixture was concentrated down to approximately 15% of the initial volume
  3. filtrationfiltered
  4. washwashing the solid with 1 L of acetonitrile
  5. concentrationThe organic liquid phase was concentrated
  6. dissolutionthe residue dissolved in 2.5 L of EtOAc
  7. washThe resulting solution was washed twice with water
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customto give a solid
  11. customThe crude was purified on a large plug of celite
  12. washelution 5% to 25% EtOAc/heptanes