Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for synthesizing phenanthridine silane derivative

A technology of phenanthridine silane and alkyl silane, applied in the field of synthesis of phenanthridine silane derivatives, can solve the problems of uneconomical reaction, expensive catalyst and the like, and achieve the effects of simple handling, efficient reaction and strong operability

Inactive Publication Date: 2014-07-23
CHANGZHOU UNIV
View PDF3 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the relatively expensive catalysts in these synthetic routes, the application of such methods is limited.
There are also reactions that require one or more times the amount of olefins to combine with the hydrogen obtained in the reaction, and the reaction is not economical.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for synthesizing phenanthridine silane derivative
  • Method for synthesizing phenanthridine silane derivative
  • Method for synthesizing phenanthridine silane derivative

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Mix 2-phenylbenzeneisonitrile 1a (2mmol), triethylsilane 2a (2mmol) and free radical initiator tert-butyl hydroperoxide (2mmol), add 10mL of benzene as a solvent, and react at room temperature in air, the reaction time Go through 4 hours. The conversion of 2-phenylbenzeneisonitrile was 100%, and the yield of 6-(triethylsilyl)phenanthridine 3aa was 80%.

Embodiment 2

[0026] Mix 2-p-tolylbenzene isocyanide 1b (2mmol), triethylsilane 2a (10mmol) and free radical initiator tert-butyl hydroperoxide (2mmol), add toluene 10mL as solvent, and react at room temperature in air. The time passes 4 hours. The conversion of 2-p-tolylbenzonitrile was 100%, and the yield of 8-methyl 6-(triethylsilyl)phenanthridine 3ba was 80%.

Embodiment 3

[0028] Mix 2-p-fluorophenylbenzeneisonitrile 1c (2mmol), triethylsilane 2a (2mmol) and free radical initiator tert-butyl hydroperoxide (20mmol), add 10mL of fluorobenzene as solvent, and react at room temperature in air , the reaction time went through 12 hours. The conversion of 2-p-fluorophenylbenzeneisonitrile was 100%, and the yield of 8-fluoro6-(triethylsilyl)phenanthridine 3ca was 68%.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a method for synthesizing a phenanthridine silane derivative, and relates to the fields of organic chemical engineering and fine chemical engineering. A small amount of organic solvent is added into 2-aryl aromatic isonitrile and silane under catalytic oxidation action of an oxidizing agent and a free radical initiator, and the mixture is subjected to cyclization reaction under the room temperature or heating condition to obtain the phenanthridine silane derivative. By using the method provided by the invention, the reaction time is 4-12 hours under the heating and stirring condition; the raw materials are reacted between the room temperature and 120 DEG C and are subjected to simple after-treatment so as to obtain the corresponding phenanthridine silane derivative with high yield of 68-93 percent. A novel aryl sp<2> silicon carbon bond formation method based on a free radical process is developed, two steps of cyclizing the free radicals and forming a silicon carbon bond are carried out to obtain a series of phenanthridine silane derivatives; therefore, the method is easy to carry out and is convenient for after-treatment.

Description

technical field [0001] The invention relates to the fields of organic chemical industry and fine chemical industry, in particular to a metal-free catalyzed radical-induced cyclization and carbon-silicon bond formation reaction, and is a novel synthesis method of phenanthridine silane derivatives. Background technique [0002] In recent years, the research on silicon-containing organic compounds has gradually increased, and the advantages of organic silicon materials have gradually become prominent. Therefore, the research on organosilanes has gradually attracted the attention of organic chemists and material scientists. Phenanthridine compounds are a class of organic compounds with azophenanthrene structure. Phenanthridine skeletons can be found in many natural product molecules and drug molecules. Drug molecules containing a phenanthridine skeleton have very good biological activities, such as being used in antibacterial, antitumor, and cytotoxic inhibition. [0003] The ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07F7/10C07F7/18
Inventor 于金涛王磊朱卉成江
Owner CHANGZHOU UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products