HRID1915748

反应详情

EQUATION

反应方程式

HRID 1915748 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

To a stirred solution of (Z)-tert-butyl 3-oxo-2,3,6,7-tetrahydro-1H-azepine-1-carboxylate (15 g, 71.1 mmol) in acetonitrile (25 mL) was added trimethylsilylazide (28.2 mL, 213 mmol) followed by Amberlite IRA 900F resin (loading: 2-3 mmol/g, 18 g) and the mixture was heated at 60° C. for 4 hr. After standing at room temperature for 16 hr, the resin was filtered off, washed with acetonitrile and the solvent removed under reduced pressure to give a yellow oil. To a solution of this oil (813 mg, 3.2 mmol) in dry Et2O (20 ml) cooled in an ice-salt bath was added a solution of methyl lithium (1.6 M in Et2O, 2.1 mL, 3.36 mmol) dropwise over 10 mins. After stirring for a further 1.5 hr, saturated NaHCO3 (10 mL) was added and the mixture was extracted with EtOAc (2×20 mL). The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure to afford a green oil (0.8 g, 81% over four steps). 1H NMR (400 MHz, CDCl3) δ 4.00-2.65 (m, 6H), 2.30-1.60 (m, 4H), 1.55-1.20 (m, 12H).

WORKUP

后处理

  1. filtrationthe resin was filtered off
  2. washwashed with acetonitrile
  3. customthe solvent removed under reduced pressure
  4. customto give a yellow oil
  5. extractionthe mixture was extracted with EtOAc (2×20 mL)
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. customthe solvent removed under reduced pressure
  8. customto afford a green oil (0.8 g, 81% over four steps)