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Synthesis of 2-Fluoro-4-iodo-anisole

Huang Suo-yi, Tian Hua

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Abstract

2-Fluoro-4-iodo-anisole was synthesized from o-amino- anisole by Schiemann reaction.Resulting in o- fluoro-anisole,then nitating and reduction at 4-position of aromatic ring followed by Sandmeyer reaction of iodo.It is the intermediate of L-3-F-tyrosine. 

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What this paper is about

2-Fluoro-4-iodo-anisole was synthesized from o-amino- anisole by Schiemann reaction.Resulting in o- fluoro-anisole,then nitating and reduction at 4-position of aromatic ring followed by Sandmeyer reaction of iodo.It is the intermediate of L-3-F-tyrosine. 

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Available abstract

2-Fluoro-4-iodo-anisole was synthesized from o-amino- anisole by Schiemann reaction.Resulting in o- fluoro-anisole,then nitating and reduction at 4-position of aromatic ring followed by Sandmeyer reaction of iodo.It is the intermediate of L-3-F-tyrosine. 

Key concepts: Anisole, Chemistry, Ring (chemistry), Medicinal chemistry, Organic chemistry, Catalysis

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