HRID58852

反应详情

EQUATION

反应方程式

HRID 58852 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A mixture of triphenylphosphine (23.3 g, 0.890 mol) and imidazole (6.0 g, 0.89 mol) in DCM (100 mL) was cooled to 0° C. and iodide (22.6 g, 0.890 mol) was added in small portions over 0.5 h. The cooling bath was removed and the mixture was stirred for 0.5 h. After the mixture was re-cooled to 0° C., a solution of Cbz-L-Ser-OMe 15.0 g, 0.590 mol) in DCM (100 mL) was added dropwise. After the addition, the cooling bath was removed and the mixture was allowed to warm to ambient temperature and stirred for 1.5 h. The mixture was filtered and the filtrate was concentrated to remove most of the solvent. MTBE (400 mL) was added to the residue and the mixture was filtered to remove triphenylphosphine oxide. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=50:1 to 10:1) to afford (R)-methyl 2-(benzyloxycarbonylamino)-3-iodopropanoate (12.3 g, 57% yield) as a colorless solid.

WORKUP

后处理

  1. customThe cooling bath was removed
  2. temperatureAfter the mixture was re-cooled to 0° C.
  3. additionAfter the addition
  4. customthe cooling bath was removed
  5. temperatureto warm to ambient temperature
  6. stirringstirred for 1.5 h
  7. filtrationThe mixture was filtered
  8. concentrationthe filtrate was concentrated
  9. customto remove most of the solvent
  10. additionMTBE (400 mL) was added to the residue
  11. filtrationthe mixture was filtered
  12. customto remove triphenylphosphine oxide
  13. concentrationThe filtrate was concentrated
  14. customthe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=50:1 to 10:1)