ac2o pyridine mechanism


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  • What is Ac 2O reagent?

    Commonly abbreviated Ac 2O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with moisture in the air.

  • Is pyridine N oxide nucleophilic?

    Pyridine N -oxide itself is generally fairly resistant to nucleophilic attack as the ring is already 'electron rich' and doesn't want to accept additional electron pairs.

  • Is pyridone missing a hydrogen?

    [Edit: nitrogen in the pyridone is missing a hydrogen. Classic error...] @orthocresol This makes a lot of sense; I was drawing parallels here to what happens in a similar reaction with an alkyl group in the alpha-position, where you do get a sigmatropic rearrangement, but it did make me blind to the last step...

  • How does a pyridine acetate react with nitrogen?

    It's worth noting that this mechanism differs significantly from the Boekelheide reaction (the initial pyridine has an additional methyl group at the 2-position), whereby the acetate bound to nitrogen is migrated by means of a [3,3] sigmatropic rearrangement.

Pyrimidine Synthesis and Salvage Pathway

Pyrimidine Synthesis and Salvage Pathway

PYRIDINE

PYRIDINE

15 Hantzsch Synthesis of Pyridine(Mechanism)

15 Hantzsch Synthesis of Pyridine(Mechanism)

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