HRID16577

反应详情

EQUATION

反应方程式

HRID 16577 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a refluxing mixture of tert-butyl 4-(aminomethyl)tetrahydro-2H-pyran-4-carboxylate (8.00 g, 0.0372 mol, step 2) and K2CO3 (0.51 g, 0.0372 mol) in EtOH-H2O (2:1, 240 mL) was added dropwise 1-ethyl-1-methyl-4-oxopiperidinium iodide (12.0 g, 0.0445 mol, J. Org. Chem. 1995, 60, 4324-4330) in EtOH-H2O (2:1, 150 mL), and the resulting mixture was stirred at the same temperature (reflux) for 1 h. After cooling to room temperature, the solvent was removed in vacuo. The residue was poured into sat. NaHCO3 aq. (200 mL), and the mixture was extracted with CH2Cl2 (200 mL×three times). The extracts were dried over Na2SO4 and concentrated. The residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (3:1 to 2:1) to give 10.77 g (98%) of the title compound as a colorless syrup.

WORKUP

后处理

  1. customthe solvent was removed in vacuo
  2. additionThe residue was poured into sat. NaHCO3 aq. (200 mL)
  3. extractionthe mixture was extracted with CH2Cl2 (200 mL×three times)
  4. dry with materialThe extracts were dried over Na2SO4
  5. concentrationconcentrated
  6. customThe residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (3:1 to 2:1)