. Pyridine on heating with sodamide gives
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Pyridine on heating with sodamide gives
C₆H₆N + NaNH₄ → C₆H₄N. NHNa + H₂
Explanation:
- The preparation of 2‐aminopyridine from pyridine and sodium amide in boiling inert solvent (such as xylene, toluene, and benzene), is generally known as the Chichibabin amination.
- It has been reported that the yield of 2‐aminopyridine depends to a large extent on the condition of the sodium amide used in the synthesis.
- A second amino group might be introduced to the aromatic ring to increase the amount of sodium amide.
- The cyclic amine has been reported to form under these conditions when the organic amine is connected to a pyridine ring.
- This reaction works not only for the pyridine series but also for other nitrogen‐containing heterocycles.
- This reaction has a general application in the preparation of nitrogen‐containing aromatic amines.
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