Bamberger triazine synthesis

The Bamberger triazine synthesis in organic chemistry is a classic organic synthesis of a triazine first reported by Eugen Bamberger in 1892.[1]

The reactants are an aryl diazonium salt obtained from reaction of the corresponding aniline with sodium nitrite and hydrochloric acid and the hydrazone of pyruvic acid. The azo intermediate converts to the benzotriazine in the third step with sulfuric acid in acetic acid.

## See also

* From the same chemist: the Bamberger rearrangement

## References

1. ↑ Hassner, A., Stumer, C., Organic Synthesis Based on Name Reactions: 2nd. Ed. Tetrahedron Organic Chemistry Series, Volume 22 Pergamon, Oxford ISBN:0-08-043260-3

* v
* t
* e

Topics in Organic Reactions

* Addition reaction
* Elimination reaction
* Polymerization
* Reagents
* Rearrangement reaction
* Redox reaction
* Regioselectivity
* Stereoselectivity
* Stereospecificity
* Substitution reaction

List of organic reactions

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Bamberger triazine synthesis. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Bamberger_triazine_synthesis&oldid=3328571"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template