Poly-aminoalkylation d'amines,en solution aqueuse ou aquo-alcoolique, à l'aide d'acides amino-2-alkylsulfuriques |
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Authors: | Joseph Rabinowitz |
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Abstract: | Alkali stable primary and secondary amines (of the types H2NCH2CH2OPO3Na2, H2NCH2COONa, H2NCH2CH2OH, H3CNHCH2CH2OH, etc.) heated with n mole-equiv. of a 2-amino-1-alkylsulfuric acid in aqueous solution, in the presence of 2 n mole-equiv. of NaOH, giverise to a mixture of poly-aminoalkylated derivatives with an average degree of aminoalkylation close to n. If the amine is insoluble in water, a mixture of water+an alcohol can be used. In the case of N-methylaminoethylsulfuric acid, the reaction is carried out in a closed vessel since the intermediate N-methylaziridine boils at 27,5° under normal pressure. These polyaminoalkyl derivatives are capable of being acylated, alkylated, and cyclized. Some stearylated products are described. |
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