HRID1008567

反应详情

EQUATION

反应方程式

HRID 1008567 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-(R)-Amino-3-isopropylsulfanyl-3-methyl-butyric acid (17 mmol; crude material obtained from D-penicillamine and isopropyl iodide) was dissolved in 40 mL of water and 40 mL of dioxane and pH 9.5 was adjusted by adding aqueous NaOH. Isopropyl chloroformate (22 mL; 1 M solution in toluene) was slowly added at 5° C. while maintaining pH 9.5 by addition of the appropriate amount of aqueous NaOH. Stirring was continued for 6 h at room temperature. Aqueous NaOH was added (pH 11) and the dioxane removed in vacuo followed by extraction of the remaining aqueous solution with ethyl acetate. KHSO4 was added and the acidified aqueous solution extracted with ethyl acetate several times. Evaporation of the solvent in vacuo gave a yellow oil, which was purified by HPLC (RP-18; pH 2.3; H2O/CH3OH 3/7) to give 3.0 g (64%) of the title compound as a colorless oil. (−)-APCI-MS: 276 ([M−H]−).

WORKUP

后处理

  1. temperaturewhile maintaining pH 9.5
  2. customthe dioxane removed in vacuo
  3. extractionfollowed by extraction of the remaining aqueous solution with ethyl acetate
  4. additionKHSO4 was added
  5. extractionthe acidified aqueous solution extracted with ethyl acetate several times
  6. customEvaporation of the solvent in vacuo
  7. customgave a yellow oil, which
  8. customwas purified by HPLC (RP-18; pH 2.3; H2O/CH3OH 3/7)