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%.
Barabanov et al. (2026) studied this question.
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