HRID252405

反应详情

EQUATION

反应方程式

HRID 252405 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 20.0 g of methyl 4-benzyloxymethyl-2-tert-butoxycarbonylamino-5-methylhexanoate [180182-92-7] in 320 ml of tetrahydrofuran at room temperature is admixed with 2.64 g of lithium borohydride in portions. After 4 hours, the reaction mixture is quenched with 200 ml of methanol dropwise over 1 hour and subsequently concentrated cautiously by evaporation. The residue is admixed once again with 150 ml of methanol and again concentrated by evaporation to dryness. The residue is admixed with 100 g of ice and 400 ml of 1N HCl and extracted with dichloromethane (3×)—the combined organic phases are washed with water, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as an beige oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.32 (1:1 EtOAc-heptane). Rt=4.96 (gradient I).

WORKUP

后处理

  1. customat room temperature
  2. customthe reaction mixture is quenched with 200 ml of methanol dropwise over 1 hour
  3. concentrationsubsequently concentrated cautiously by evaporation
  4. concentrationagain concentrated by evaporation to dryness
  5. extractionextracted with dichloromethane (3×)—the combined organic phases
  6. washare washed with water
  7. dry with materialdried over sodium sulphate
  8. concentrationconcentrated by evaporation