Home Chemistry Organic Building Blocks Nitroes Methyl 4-Amino-3-Nitrobenzoate
These compounds have the same murcko framework: benzene,and at least 3 kinds of functional groups( —NO2,—NH2,—COOCH3).
Halogenation: Nitrobenzene can undergo halogenation reactions, where halogen atoms (such as chlorine or bromine) are substituted onto the benzene ring. This is usually achieved using halogenating agents in the presence of a catalyst.
Reimer-Tiemann Reaction: Aniline can react with chloroform (CHCl3) and a base to undergo the Reimer-Tiemann reaction, leading to the formation of a salicylaldehyde derivative.
Reduction: Methyl benzoate can be reduced to benzyl alcohol using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4). The ester functional group is reduced to an alcohol functional group.
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Methyl 4-amino-3-chloro-5-nitrobenzoate
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Methyl 2,4-diamino-3-fluoro-5-nitrobenzoate
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Methyl 4-amino-3-methyl-5-nitrobenzoate
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Methyl 4-amino-5-chloro-2-methoxy-3-nitrobenzoate
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Methyl 4-amino-2-methoxy-5-nitrobenzoate
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Methyl 4-amino-2,3-difluoro-5-nitrobenzoate
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