HRID1017120

反应详情

EQUATION

反应方程式

HRID 1017120 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of (±)1-Amino-2-phenylethyl phosphonous acid (19) (70 mmol) in dioxane (200 mL) and aqueous 1 M NaOH (75 mL) at 0° C. was added dropwise benzyl chloroformate (20 mL). The pH of the solution during this addition was kept at 8-9 with the simultaneous addition of aqueous 1M NaOH (75 mL). The reaction mixture was stirred at room temperature for a further 16 hours and then was concentrated in vacuo to half volume. Washed with diethyl ether (2×75 mL) and then acidified to pH1 with the addition of concentrated aqueous hydrochloric acid. Extracted with ethyl acetate (3×80 mL) and the combined organic phases were washed with water (1×20 mL), dried over anhydrous MgSO4, filtered and evaporated in vacuo which gave (±)N-CBZ-1-amino-2-phenylethyl phosphonous acid (20) (15.44 g).

WORKUP

后处理

  1. additionThe pH of the solution during this addition
  2. concentrationwas concentrated in vacuo to half volume
  3. washWashed with diethyl ether (2×75 mL)
  4. additionacidified to pH1 with the addition of concentrated aqueous hydrochloric acid
  5. extractionExtracted with ethyl acetate (3×80 mL)
  6. washthe combined organic phases were washed with water (1×20 mL)
  7. dry with materialdried over anhydrous MgSO4
  8. filtrationfiltered
  9. customevaporated in vacuo which