HRID2193047

反应详情

EQUATION

反应方程式

HRID 2193047 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 5 mL of a dichloromethane solution containing 0.66 g of tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate, 5 mL of trifluoroacetic acid was added, and the mixture was stirred at room temperature for 1 hour. The solvent was removed under reduced pressure, and thereto were added chloroform, water and 6 mol/L hydrochloric acid. The aqueous layer was separated, and the aqueous layer was washed with chloroform. Chloroform was added to the aqueous layer, and the resultant solution was adjusted to pH 13 with a 20% aqueous sodium hydroxide solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.26 g of a colorless oily substance, N-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-4-methylpiperidine-4-amine.

WORKUP

后处理

  1. additionwas added
  2. customThe solvent was removed under reduced pressure
  3. additionwere added chloroform, water and 6 mol/L hydrochloric acid
  4. customThe aqueous layer was separated
  5. washthe aqueous layer was washed with chloroform
  6. additionChloroform was added to the aqueous layer
  7. customThe organic layer was separated
  8. extractionthe aqueous layer was extracted with chloroform
  9. dry with materialthe resultant solution was dried over anhydrous magnesium sulfate
  10. customthe solvent was removed under reduced pressure