HRID51272

反应详情

EQUATION

反应方程式

HRID 51272 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of veratrole (16.6 g, 0.120 mol) in tetrahydrofuran (130 mL) at −78° C. was added n-butyllithium (50.5 mL, of a 2.5 M solution in hexane, 0.126 mmol). The resulting mixture was allowed to warm to ambient temperature over 1 hour and then stirred at this temperature for 4 hours before recooling to −78° C. and treating the resulting slurry with a solution of 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) (30.71 g, 0.1128 mol) in tetrahydrofuran (180 mL). The reaction mixture was allowed to warm slowly to ambient temperature overnight and then recooled to 0° C. and quenched by the addition of saturated aqueous ammonium chloride solution (110 mL). The aqueous layer was extracted with ether (110 mL) and the combined organic extracts were washed with brine (220 mL), dried (MgSO4) and concentrated in vacuum to give the title compound (7).

WORKUP

后处理

  1. custombefore recooling to −78° C.
  2. temperatureto warm slowly to ambient temperature overnight
  3. customrecooled to 0° C.
  4. customquenched by the addition of saturated aqueous ammonium chloride solution (110 mL)
  5. extractionThe aqueous layer was extracted with ether (110 mL)
  6. washthe combined organic extracts were washed with brine (220 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuum