Secondary and tertiary amines derived from pelargonaldehyde and methyl azelaaldehydate View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1969-02

AUTHORS

E. H. Pryde, D. E. Anders, J. C. Cowan

ABSTRACT

Reductive alkylation of ammonia with pelargonaldehyde or with methyl azelaaldehydate over Raney nickel catalyst produced dinonylamine or bis(8-carbomethoxyoctyl)amine in good yields. Tertiary amine formation was minimized by the use of two immiscible solvents. When 10% palladium on charcoal was used in place of the nickel catalyst, trinonylamine and tris(8-carbomethoxyoctyl)amine were formed in good yield in the absence of solvents. More... »

PAGES

67-69

References to SciGraph publications

  • 1963-12. Methyl azelaaldehydate purification via the bisulfite compound in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1965-03. Omega-formylalkanoates by ozonization of unsaturated fatty esters in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1968-02. Laboratory optimization of process variables in reductive ozonolysis of methyl soyate in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
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    URI

    http://scigraph.springernature.com/pub.10.1007/bf02541210

    DOI

    http://dx.doi.org/10.1007/bf02541210

    DIMENSIONS

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