HRID234089

反应详情

EQUATION

反应方程式

HRID 234089 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 12.0 g (0.033 mol) of (1g) in 25 ml of dichloromethane was cooled with an ice bath and 25 ml of trifluoroacetic acid was added. The solution was stirred at ca 5° C. for 20 minutes, then allowed to stir to room temperature. After 90 minutes, the dichloromethane and trifluoroacetic acid were removed in vacuo. The resulting residue was dissolved in 200 ml of ethyl acetate and washed with 2M sodium hydroxide (200 ml) and brine (100 ml). After drying over anhydrous magnesium sulfate, the solution was filtered and concentrated in vacuo to produce 7.86 g (90% yield) of L-alanine, 2-(benzyloxycarbonylamino)ethyl amide (1h) as a white solid. 1H NMR (CDCl3) δ 1.28(d, 3H), 2.09(m, 2H), 3.33(m, 4H), 3.47(q, 1H), 5.07(s, 2H), 5.59(bt, 1H), 7.33(bs, 5H), 7.69(bt, 1H); 13C NMR (CDCl3) δ 21.3, 39.5, 40.9, 50.4, 66.6, 128.0, 128.1, 128.4, 136.4, 156.9, 176.7.

WORKUP

后处理

  1. stirringto stir to room temperature
  2. waitAfter 90 minutes
  3. customthe dichloromethane and trifluoroacetic acid were removed in vacuo
  4. dissolutionThe resulting residue was dissolved in 200 ml of ethyl acetate
  5. washwashed with 2M sodium hydroxide (200 ml) and brine (100 ml)
  6. dry with materialAfter drying over anhydrous magnesium sulfate
  7. filtrationthe solution was filtered
  8. concentrationconcentrated in vacuo