The Preparation of Some New Polyfunctional Organic Azides,

Abstract

3,3-Diazido-2,4-dinitratopentane was prepared from 2.4-pentanedione by (1) Cu-(OAc)2-catalyzed dibromination (2) displacement of bromines by azide with sodium azide in acetonitrile (3) carbonyl reduction with LAH or sodium borohydride and (4) nitration with acetyl nitrate. Also, 2,3-diazido-1,4-dinitratobutane was prepared from 2-butene-1,4-diol by (1) addition of iodine azide (2) iodine displacement with aqueous sodium azide and (3) nitration with acetyl nitrate. The diazidodinitrates were obtained as mixtures of solid and liquid isomers. The solids are similar to fulminate of mercury in impact sensitivity and begin rapid thermal decomposition at approximately 145C. Films made from the diazidodinitrates and nitrocellulose are clear, tough and flexible. Their impact sensitivities and thermal analyses are comparable to those of standard NG-NC propellants. (Author)

Document Details

Document Type
Technical Report
Publication Date
Sep 01, 1972
Accession Number
AD0751762

Entities

People

  • Alan C. Duckworth
  • Lester P. Kuhn

Organizations

  • Ballistic Research Laboratory

Tags

DTIC Thesaurus Topics

  • Acetonitrile
  • Alkenes
  • Azides
  • Displacement
  • Nitration
  • Nitriles
  • Sensitivity
  • Sodium
  • Sodium Azides
  • Sodium Compounds
  • Thermal Analysis

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Rocket Propulsion.