HRID609646

反应详情

EQUATION

反应方程式

HRID 609646 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-10 °C

PROCEDURE

实验过程

To a solution of bromoacetyl bromide (0.25 mL, 2.92 mmol) in CH2Cl2 (10 mL) at -10° C. was added a solution of 2-(phenylethylamino)ethyl carbamic acid tert-butyl ester (0.7 g, 2.65 mmol) and triethylamine (0.41 mL, 2.92 mmol) in CH2Cl2 (10 mL) dropwise. The mixture was stirred at -10° C. for 30 min, before removal of the solvent in vacuo. The residue was partitioned between EtOAc (2×30 mL) and water (30 mL). The combined organic layers were dried (Na2SO4) and evaporated. The residue was chromatographed on silica gel, eluting with petrol:EtOAc (2:1→1:1), to afford the title amide (0.81 g, 79%) as a colourless oil. 1H NMR (250 MHz, CDCl3) δ 1.44 (9H, s), 2.86-2.94 (2H, m), 3.10-3.94 (8H, m), 4.59 and 4.92 (1H, 2×br s), 7.15-7.37 (5H, m). MS (ES+) (385/387, M+).

WORKUP

后处理

  1. customThe residue was partitioned between EtOAc (2×30 mL) and water (30 mL)
  2. dry with materialThe combined organic layers were dried (Na2SO4)
  3. customevaporated
  4. customThe residue was chromatographed on silica gel
  5. washeluting with petrol:EtOAc (2:1→1:1)