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March 15, 2026Russian Journal of General Chemistry0 citations

Effective Synthesis of α,ω-Diaminoalkanes by the Optimized Gabriel Method

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MBMikhail A. BarabanovGMGeorgy S. MartyanovAPAlexander V. Pestov

Key Points

  • The aim is to optimize the Gabriel method for synthesizing α,ω-diaminoalkanes.
  • Alkylation of phthalimide with α,ω-dibromoalkanes in dimethylformamide.
  • Use of anhydrous potassium carbonate as a base.
  • Hydrolysis of the resulting dibromoalkanes in potassium hydroxide.
  • Steam distillation to isolate diamine bases.
  • Neutralization of distillate with hydrochloric acid.
  • Successful conversion of phthalimide to α,ω-diaminoalkanes.
  • Overall yields of 90–96% for the target dihydrochlorides.

Abstract

Alkylation of phthalimide with α,ω-dibromoalkanes in dimethylformamide in the presence of anhydrous potassium carbonate afforded a series of α,ω-diphthalimidoalkanes. Their subsequent hydrolysis in a potassium hydroxide solution, steam distillation of the diamine bases, and neutralization of the distillate with hydrochloric acid yielded the target α,ω-diaminoalkanes as dihydrochlorides with overall yields of 90–96%.

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Cite This Study

Barabanov et al. (2026) studied this question.

synapsesocial.com/papers/69b64c67b42794e3e660dc09https://doi.org/10.1134/s1070363225606787
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