HRID1183556

反应详情

EQUATION

反应方程式

HRID 1183556 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of the 2-benzyl-N-benzyloxy-malonamic acid ethyl ester (19 g, 58.1 mmol) dissolved in a mixture of THF (70 mL) and MeOH (200 mL) was added a solution of NaOH (5.4 g, 135 mmol) in water (100 mL). The mixture was stirred at room temperature for 24 hours, and evaporated to remove volatile organic solvents. The aqueous residue was diluted with water (200 mL), and washed with DCM (200 mL). The aqueous layer was saved and acidified to pH˜4 by adding concentrated HCl. The desired product was precipitated, washed with water, dissolved in acetone (200 mL), and evaporated to dryness, affording intermediate (12a) as a white solid (14.2 g). 1H-NMR (CD3OD, 300 MHz) δ(ppm) 7.20-7.06 (m, 5H), 4.60-4.56 (d, 1H), 4.42-4.38 (d, 1H), 3.10-2.98 (m, 2H).

WORKUP

后处理

  1. customevaporated
  2. customto remove volatile organic solvents
  3. additionThe aqueous residue was diluted with water (200 mL)
  4. washwashed with DCM (200 mL)
  5. additionby adding concentrated HCl
  6. customThe desired product was precipitated
  7. washwashed with water
  8. dissolutiondissolved in acetone (200 mL)
  9. customevaporated to dryness