HRID2169282

反应详情

EQUATION

反应方程式

HRID 2169282 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a stirred suspension of NH4Cl (1.3 g, 23.69 mmol) in dry toluene (30 mL) was added trimethylaluminium (2M solution in toluene) dropwise at 0° C., stirred at 0° C. for 15 min, then stirred at room temperature for 2 h. The solution of [1-(4-trifluoromethyl-phenyl)-cyclopentyl]-acetonitrile (241) (2 g, 7.89 mmol) in toluene (10 mL) was added dropwise at the room temperature and the reaction mixture was heated at 80° C. for 16 h, the reaction mixture was cooled to 0° C., and the reaction mixture was poured into the slurry of silica gel (4 g) in CHCl3 (4 mL), stirred vigorously for 30 min at 0° C., the solid was filtered off through celite and washed with methanol (5×100 mL). The filtrate was concentrated and the crude product was taken up in 10% methanol in dichloromethane (200 mL) and stirred for 30 min. The solid was discarded by filtration and the filtrate was concentrated. The crude product was suspended in ether and a solid was collected by filtration and dried to get 2-(1-p-tolyl-cyclopentyl)-acetamidine (hydrochloride salt) (242) (1.4 g, 65.59%) as a light yellow solid.

WORKUP

后处理

  1. stirringstirred at room temperature for 2 h
  2. temperaturethe reaction mixture was heated at 80° C. for 16 h
  3. temperaturethe reaction mixture was cooled to 0° C.
  4. stirringstirred vigorously for 30 min at 0° C.
  5. filtrationthe solid was filtered off through celite
  6. washwashed with methanol (5×100 mL)
  7. concentrationThe filtrate was concentrated
  8. stirringstirred for 30 min
  9. filtrationThe solid was discarded by filtration
  10. concentrationthe filtrate was concentrated
  11. filtrationa solid was collected by filtration
  12. customdried