P-aminophenol react with acetyl chloride in presence of pyridine to give
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I want to devise the synthesis of 1,2-dinitrobenzene without producing a large amount of 1,3 or 1,4 products.
In my synthesis I have a step in which I obtain aniline. I would like to know the mechanism for protecting the amine using CH3COCl and triethylamine so I can keep it from reacting in the next step of my synthesis. I'm not really "fluent" with amine chemistry, and I have no good idea at the moment.
If you cannot make picture of mechanism, please explain it with words. I must understand!
In my synthesis I have a step in which I obtain aniline. I would like to know the mechanism for protecting the amine using CH3COCl and triethylamine so I can keep it from reacting in the next step of my synthesis. I'm not really "fluent" with amine chemistry, and I have no good idea at the moment.
If you cannot make picture of mechanism, please explain it with words. I must understand!