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	<PublisherName>International Science Community Association</PublisherName>

	<JournalTitle>Research Journal of Chemical Sciences</JournalTitle> 

	<Issn>2231 - 606X</Issn>

	<Volume>5</Volume>

	<Issue>12</Issue>

	<PubDate PubStatus="ppublish"> 

	<Year>2015</Year> 

	<Month>December</Month> 

	<Day>18</Day> 

	</PubDate>

	</Journal>



	<ArticleTitle>Chlorination of Aromatic Compounds in Aqueous Media using N-Chlorosuccinimide</ArticleTitle> 


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		<Affiliation>CIMFR Nagpur Unit-II, 17/C-Telenkhedi area, Civil Lines, Nagpur, 440001, INDIA Hislop college, Civil lines, Nagpur-440001, INDIA</Affiliation>

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		<Affiliation> Laboratory of Inorganic Chemistry and Environment (LACIE), Faculty of Sciences and Technics (FAST), University of Abomey-Calavi, 01 BP </Affiliation>

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		<LastName>Daouda</LastName>

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		<FirstName>AINA</FirstName>

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	<PublicationType>Research Paper</PublicationType>


	<History>  
	<PubDate PubStatus="received">
	<Year>2015</Year>
	<Month>7</Month>
	<Day>30</Day>
	</PubDate>
	<PubDate PubStatus="accepted">										
	<Year>2015</Year> 
	<Month>December</Month>									
	<Day>18</Day> 
	</PubDate>

	</History>
	<Abstract>A proficient/effective method for the synthesis of chlorinated arenes is revealed. The system involves the use of N-Chlorosuccinimide (NCS) as chlorinating and oxidizing agent in aqueous medium under mild conditions to chlorinate the aromatic compounds in virtuous to excellent yields (75-96 percent). The reagent system is efficient, organic solvent-free and easy to handle. N-Chlorosuccinimide is an advantageous reagent for aromatic halogenation, while at the same time, circumventing electrophilic addition of chlorine to a pi bond.  </Abstract>

	<CopyrightInformation>Copyright@ International Science Community Association</CopyrightInformation>

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