HRID2363366

反应详情

EQUATION

反应方程式

HRID 2363366 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 735 mg (3 mmol) of N-Boc-4-hydroxyproline methyl ester in 20 mL of THF stirred at 0° C. was added 79 mg (1.1 eq, 3.3 mmol) of 60% sodium hydride in mineral oil. The mixture was stirred at 0° C. for 1 hour, and methyl iodide (0.56 mL, 3 eq, 9 mmol) was added. The mixture was stirred at room temperature overnight, quenched by addition of saturated aqueous ammonium chloride, diluted with water, and extracted with three 80 mL portions of ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4), and concentrated in vacuo to afford a pale yellow oil. The oil was taken up in 9 mL of CH3OH and 3 mL of water, and 378 mg (3 eq, 9 mmol) of lithium hydroxide was added. The mixture was stirred at room temperature overnight, diluted with water, acidified to pH 3 and extracted with three 80 mL portions of ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. The residual oil was taken up in 10 mL of TFA and the solution was stirred at room temperature for 2 hours, and concentrated in vacuo. The residual oil was diluted with 6 mL of 10% aqueous sodium carbonate and 3 mL of dioxane, and a solution of 9-fluorenylmethyl chloroformate (779 mg, 1 eq, 3 mmol) in 5 mL of dioxane was added. The mixture was stirred at room temperature overnight, diluted with water, acidified to pH 3 and extracted with three 80 mL portions of ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo to afford an oil, which was purified by column chromatography over silica gel eluted with CH2Cl2/CH3OH 20:1, to afford 600 mg (55%) of N-Fmoc-4-methoxyproline: exact mass calculated for C21H21NO5 m/e 367.14 found m/e 368.4.

WORKUP

后处理

  1. stirringThe mixture was stirred at room temperature overnight
  2. customquenched by addition of saturated aqueous ammonium chloride
  3. additiondiluted with water
  4. extractionextracted with three 80 mL portions of ethyl acetate
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customto afford a pale yellow oil
  9. stirringThe mixture was stirred at room temperature overnight
  10. extractionextracted with three 80 mL portions of ethyl acetate
  11. washThe combined organic extracts were washed with brine
  12. dry with materialdried (MgSO4)
  13. concentrationconcentrated in vacuo
  14. stirringthe solution was stirred at room temperature for 2 hours
  15. concentrationconcentrated in vacuo
  16. additionThe residual oil was diluted with 6 mL of 10% aqueous sodium carbonate and 3 mL of dioxane
  17. stirringThe mixture was stirred at room temperature overnight
  18. extractionextracted with three 80 mL portions of ethyl acetate
  19. washThe combined organic extracts were washed with brine
  20. dry with materialdried (MgSO4)
  21. concentrationconcentrated in vacuo
  22. customto afford an oil, which
  23. customwas purified by column chromatography over silica gel
  24. washeluted with CH2Cl2/CH3OH 20:1