ChemicalBook--->CAS DataBase List--->477776-17-3

477776-17-3

477776-17-3 Structure

477776-17-3 Structure
IdentificationBack Directory
[Name]

Quinoxaline, 6-(chloromethyl)-
[CAS]

477776-17-3
[Synonyms]

6-(Chloromethyl)quinoxaline
Quinoxaline, 6-(chloromethyl)-
[Molecular Formula]

C9H7ClN2
[MDL Number]

MFCD15144408
[MOL File]

477776-17-3.mol
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
Hazard InformationBack Directory
[Synthesis]

6-Methylquinoxaline

6344-72-5

Quinoxaline,  6-(chloromethyl)-

477776-17-3

The general procedure for the synthesis of 6-(chloromethyl)quinoxaline from 6-methylquinoxaline is as follows: Example 1: Catalytic air dehydrogenation of 6-hydroxymethyl-methyl-quinoxaline In a 500 mL round-bottomed flask, 6-methylquinoxaline (10 g, 69.4 mmol) was dissolved in 240 g of acetonitrile with N-chlorosuccinimide (14 g, 105.3 mmol). Benzoyl peroxide (0.4 g, 1.65 mmol) was added as initiator. A reflux condenser was installed and the reaction mixture was heated and refluxed for 6 hours, followed by the addition of benzoyl peroxide (0.1 g). The reflux reaction was continued for a total reaction time of 12 hours. Upon completion of the reaction, the reaction solution was analyzed by gas chromatography (GC), which showed the generation of 6-(chloromethyl)quinoxaline with 80% selectivity and 60% conversion.

[References]

[1] Patent: US6559308, 2003, B1
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