反应 #67952

ord-c846f63164644d04a5a0217a7ae5a053

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.STIRRINGstirred at the same temperature for 30 minutes
  3. 3
    workup.STIRRINGstirred at the same temperature for 30 minutes
  4. 4
    workup.STIRRINGthe reaction mixture was stirred for 1 hour
  5. 5
    温度under reflux
  6. 6
    温度by heating
  7. 7
    其他The organic layer was separated
  8. 8
    萃取the aqueous layer was extracted with chloroform
  9. 9
    洗涤the resultant solution was washed with an aqueous saturated sodium chloride solution
  10. 10
    干燥dried over anhydrous magnesium sulfate
  11. 11
    其他the solvent was removed under reduced pressure

实验过程

To 5 mL of a dichloromethane solution containing 0.50 g of tert-butyl 4-amino-4-methylpiperidine-1-carboxylate, 0.38 g of 2,3-dihydro-1,4-benzodioxin-6-carbaldehyde and 0.13 mL of acetic acid were added, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes, and then the reaction mixture was stirred for 1 hour under reflux by heating. Thereto were added chloroform and an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, and the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.81 g of a light brown oily substance, tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08524738B2uspto-grants-2013_09