HRID527214

反应详情

EQUATION

反应方程式

HRID 527214 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4M HCl/dioxane (5.49 ml, 22.0 mmol) was added to a solution of (S)-3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoic acid (0.329 g, 1.10 mmol) in 2:1 dioxane:DCM (10 mL). The reaction mixture was stirred at room temperature overnight (16 hours), after which it was concentrated to ⅓ volume. The resulting cloudy mixture was diluted with ether, and the mixture was concentrated again to ⅓ volume. The mixture was diluted again with ether (20 mL), and the solids were isolated by filtration through a medium frit funnel with nitrogen pressure, rinsed with ether (5×10 mL), dried under nitrogen pressure, and dried in vacuo to give (S)-3-amino-2-(4-chlorophenyl)propanoic acid hydrochloride (0.199 g, 76.8% yield) as a white powder. HPLC >99 area % pure. LC/MS (APCI+) m/z 200.

WORKUP

后处理

  1. concentrationafter which it was concentrated
  2. additionThe resulting cloudy mixture was diluted with ether
  3. concentrationthe mixture was concentrated again
  4. additionThe mixture was diluted again with ether (20 mL)
  5. customthe solids were isolated by filtration through a medium frit funnel with nitrogen pressure
  6. washrinsed with ether (5×10 mL)
  7. customdried under nitrogen pressure
  8. customdried in vacuo