HRID1814406

反应详情

EQUATION

反应方程式

HRID 1814406 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a stirred suspension of K2CO3 (200 g, 1.5 mole) in cyclohexane 200 mL and 1-bromo-3-chloropropane (540 gms, 3.4 mole) is added dropwise over a period of 1 h at 20° C. di-t-butyl amine (289 g, 2.24 mole). After complete addition the reaction is allowed to stir for an additional 20 h. The crude reaction mixture is filtered and then washed with saturated NaCl (3×100 mL). The organic phase is extracted with 3N HCl (3×100 mL). The resulting aqueous phase, containing the desired product as the hydrochloric salt, is washed with hexanes (3×100 mL) to remove any residual BCP. The aqueous phase is subsequently basified with 50 wt % NaOH and extracted with cyclohexane (3×100 mL). After solvent removal 234 g (51% yield) of the title compound is isolated as a yellow oil.

WORKUP

后处理

  1. additionAfter complete addition the reaction
  2. customThe crude reaction mixture
  3. filtrationis filtered
  4. washwashed with saturated NaCl (3×100 mL)
  5. extractionThe organic phase is extracted with 3N HCl (3×100 mL)
  6. additionThe resulting aqueous phase, containing the desired product as the hydrochloric salt
  7. washis washed with hexanes (3×100 mL)
  8. customto remove any residual BCP
  9. extractionextracted with cyclohexane (3×100 mL)