HRID1005643

反应详情

EQUATION

反应方程式

HRID 1005643 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

6.70 ml of n-BuLi (16.8 mmol) were added dropwise at 100° C. to 3.50 g of o-bromoquinoline (16.8 mmol) dissolved in 50 ml of THF, and the mixture was subsequently stirred at 80° C. for 15 minutes. A solution of 50 ml of THF and 2.45 g of 2-methyl-1-indanone (16.8 mmol) was then added to the lithiated bromoquinoline over the course of 10 minutes. The mixture was allowed to cool to room temperature, and the solution was then refluxed for three hours, cooled to room temperature, acidified to pH 1 using ice and hydrochloric acid and subsequently refluxed for three hours. The reaction mixture was adjusted to pH 9 using ammonia solution, and the aqueous phase was extracted with diethyl ether. The combined organic phases were dried, and the solvent was removed. The crude product was purified by distillation under reduced pressure at 150-160° C./10−2 mbar, giving 1.5 g of 1-(8-quinolyl)-2-methylindene (45%) as a yellow, viscous resin.

WORKUP

后处理

  1. temperatureto cool to room temperature
  2. temperaturethe solution was then refluxed for three hours
  3. temperaturecooled to room temperature
  4. temperaturesubsequently refluxed for three hours
  5. extractionthe aqueous phase was extracted with diethyl ether
  6. customThe combined organic phases were dried
  7. customthe solvent was removed
  8. distillationThe crude product was purified by distillation under reduced pressure at 150-160° C./10−2 mbar