Cyanoethylation of Some Alkanolamines

Abstract

The paper describes the preparation of a series of alkanolamines (HO- R-NH2) bearing one or two cyanoethyl (-C2H4CN) groups on the amino nitrogen. Choice of reaction conditions and certain structural features determine whether mono- or disubstitution occurs, and when both products are formed, the mixture may be conveniently analysed by non-aqueous titration. All products have been characterised as p-nitrobenzoyl derivatives.

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Document Details

Document Type
Technical Report
Publication Date
Jul 12, 1971
Accession Number
AD0744758

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  • C. Kenworthy
  • J. A. Bell

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DTIC Thesaurus Topics

  • Acetic Acid
  • Acids
  • Alcohols
  • Alkenes
  • Explosives
  • Hydrochloric Acid
  • Hydrogen
  • Internal Pressure
  • Low Temperature
  • Materials
  • Molecular Weight
  • New York
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  • Spectra
  • Stainless Steel
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  • Chemistry

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  • Organic Chemistry