反应 #6304

ord-f11fb9357654407f897a52ae5b73be5e

反应条件

温度
90°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度heating
  2. 2
    温度After cooling to room temperature
  3. 3
    萃取the mixture is extracted with three portions of ether
  4. 4
    干燥The combined organics are dried over 4A sieves
  5. 5
    过滤filtered through cotton
  6. 6
    其他evaporated
  7. 7
    其他The crude reaction product
  8. 8
    萃取After careful neutralization with saturated sodium bicarbonate, the aqueous mixture is extracted with three portions of ether
  9. 9
    干燥dried over 4A sieves
  10. 10
    过滤filtered through cotton
  11. 11
    其他evaporated

实验过程

To a solution 30.3 g (0.1 mole) of N-acetoxyhexyl-1,2,3,4-tetrahydroquinoline-6-carboxaldehyde in dimethylformamide is added 7.4 g (0.2 mole) of 1,3-dioxolan-2-ylmethyltributylphosphonium bromide in dimethylformamide with magnetic stirring, and the mixture is heated at 90° C. Potassium t-butoxide (22.4 g, 0.2 mole) is added, and heating is continued at 90° C. for 16 hours. After cooling to room temperature, the solution is poured into a seven-fold excess of water. The aqueous mixture is saturated with sodium chloride, and the mixture is extracted with three portions of ether. The combined organics are dried over 4A sieves, filtered through cotton, and evaporated. The crude reaction product is then dissolved in 3M HCl, and the reaction is stirred at room temperature for 16 hours. After careful neutralization with saturated sodium bicarbonate, the aqueous mixture is extracted with three portions of ether, and the combined organics are passed through silica gel, dried over 4A sieves, filtered through cotton, and evaporated to yield 3-(N-hydroxyhexyl-1,2,3,4-tetrahydroquinolin-6-yl)acrolein.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05247042uspto-grants-1993_09