反应 #1483120

ord-018ed051f7d64bb4b6564448c9796a03

反应方程式

Oc1ccccc1-c1ccc2ccc3cccnc3c2n1
2-(2-Hydroxyphenyl)-1,10-phenanthroline
Oc1ccccc1-c1ccc2ccc3cccnc3c2n1
2-(2-Hydroxyphenyl)-1,10-Phenanthroline
CC(C)(C)[O-].[Li+]
lithium t-butoxide
[Li+].[O-]c1ccccc1-c1ccc2ccc3cccnc3c2n1
Lithium 2-(1,10-Phenanthrolin-2-yl)-Phenolate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGThe precipitated product was stirred at room temperature in the reaction mixture for 1 hour
  2. 2
    其他the reaction
  3. 3
    过滤The lithium 2-(1,10-phenanthrolin-2-yl)-phenolate was filtered off
  4. 4
    洗涤washed well with diethyl ether
  5. 5
    其他air-dried

实验过程

2-(2-Hydroxyphenyl)-1,10-phenanthroline (4) (20 g, 73.45 mMole) was dissolved in tetrahydrofuran and with good stirring treated with lithium t-butoxide (5.65 g, 88.14 mMole). The precipitated product was stirred at room temperature in the reaction mixture for 1 hour to complete the reaction. The lithium 2-(1,10-phenanthrolin-2-yl)-phenolate was filtered off, washed well with diethyl ether and air-dried. Yield 21 g.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08900722B2uspto-grants-2014_12