HRID1701054

反应详情

EQUATION

反应方程式

HRID 1701054 的结构方程式

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

((1R)-1-Benzyl-2,5-dihydroxypentyl)methylcarbamic acid tert-butylester (560 mg, 1.52 mmol) was dissolved in ethyl acetate (10 mL). 3M Hydrogen chloride in ethyl acetate (2.0 mL, 6.08 mmol) was added. The solution was stirred at room temp. for 1 h. It was diluted with ethyl acetate (10 mL) and extracted with 1N sodium hydroxide solution (30 mL). The aqueous phase was extracted with ethyl acetate (3×10 mL). The combined organic phases were dried over magnesium sulfate. The solvent was removed in vacuo. The residue was dissolved in dichloromethane (5 mL). The solution was cooled to 0° C. Trifluoroacetic acid (5 mL) was added. The solution was stirred at this temp. for 5 min. The solvents were removed in vacuo. The residue was dissolved in ethyl acetate (10 mL). The solution was extracted with iN sodium hydroxide solution (10 mL). The aqueous phase was extracted with ethyl acetate (2×5 mL). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (40 g) with dichloromethane/methanol/25% aqueous ammonia 100:10:1 to give 136 mg of (5R)-4-hydroxy-5-(methylamino)-6-phenylhexyl acetate.

WORKUP

后处理

  1. extractionextracted with 1N sodium hydroxide solution (30 mL)
  2. extractionThe aqueous phase was extracted with ethyl acetate (3×10 mL)
  3. dry with materialThe combined organic phases were dried over magnesium sulfate
  4. customThe solvent was removed in vacuo
  5. dissolutionThe residue was dissolved in dichloromethane (5 mL)
  6. additionTrifluoroacetic acid (5 mL) was added
  7. stirringThe solution was stirred at this temp
  8. waitfor 5 min
  9. customThe solvents were removed in vacuo
  10. dissolutionThe residue was dissolved in ethyl acetate (10 mL)
  11. extractionThe solution was extracted with iN sodium hydroxide solution (10 mL)
  12. extractionThe aqueous phase was extracted with ethyl acetate (2×5 mL)
  13. dry with materialThe combined organic layers were dried over magnesium sulfate
  14. customThe solvent was removed in vacuo
  15. customThe crude product was purified by flash chromatography on silica (40 g) with dichloromethane/methanol/25% aqueous ammonia 100:10:1