Leuckart reaction of carbonyl derivatives of 2,6-di-tert-butylphenol View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1985-06

AUTHORS

G. F. Bannikov, G. A. Nikiforov, V. V. Ershov

ABSTRACT

Conclusions1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethylamine and its analogs were prepared in high yield by the Leuckart reaction from the corresponding ketones or aldehyde and ammonium formate or formamide.The reaction of α-methyl-2,6-di-tert-butylmethylquinone with ammonia leads to 1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethylamine.

PAGES

1289-1291

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00956104

DOI

http://dx.doi.org/10.1007/bf00956104

DIMENSIONS

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