Aromatic chlorination of ω-phenylalkylamines and ω-phenylalkylamides in carbon tetrachloride and α,α,α-trifluorotoluene
Date
2006
Authors
O'Connell, Jenny
Simpson, Jamie S
Dumanski, Paul
Simpson, Gregory Wayne
Easton, Christopher
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Royal Society of Chemistry
Abstract
The aromatic halogenation of simple alkylbenzenes with chlorine proceeds smoothly in acetic acid but is much less efficient in less polar solvents. By contrast chlorination of ω-phenylalkylamines, such as 3-phenylpropylamine, occurs readily in either ace
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Keywords: Acetic acid; Amines; Carbon inorganic compounds; Organic solvents; Rate constants; Alkylbenzenes; O-chloroimidates; Ortho-chlorinated products; Aromatic compounds; alpha,alpha,alpha trifluorotoluene; alpha,alpha,alpha-trifluorotoluene; amide; carbon tetra
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Organic and Biomolecular Chemistry
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Journal article
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2037-12-31
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