HRID1836715

反应详情

EQUATION

反应方程式

HRID 1836715 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

7.4 g of benzyl-[2-(2-methoxy-phenoxy)-ethyl]-amine (29 mmol) were dissolved in 47 ml ethanol. To the stirred solution 10 g of 9-benzenesulfonyl-4-oxiranylmethoxy-9H-carbazole (26 mmol) were added and the mixture was heated under reflux for 15 h. The boiling solution was treated with 1 g of activated carbon for 30 min. The activated carbon was filtered off in the heat, and washed with 20 ml ethanol. The ethanol was rotary evaporated (Tbath 40° C., 20 mbar) and the crude material purified by liquid chromatography (eluent toluene/ethyl acetate 4:1), the pure fractions were collected and rotary evaporated (40° C./15 mbar).

WORKUP

后处理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 15 h
  3. additionThe boiling solution was treated with 1 g of activated carbon for 30 min
  4. filtrationThe activated carbon was filtered off in the heat
  5. washwashed with 20 ml ethanol
  6. customThe ethanol was rotary evaporated (Tbath 40° C., 20 mbar)
  7. customthe crude material purified by liquid chromatography (eluent toluene/ethyl acetate 4:1)
  8. customthe pure fractions were collected
  9. customrotary evaporated (40° C./15 mbar)