Preparation of N,N'-Dicarboxymethyl-1,3-propanediamines

Details Preparation of N,N'-Dicarboxymethyl-1,3-propanediamines Preparation of N,N'-Dicarboxymethyl-1,3-propanediamines

1976-07-07

1977-11-15

Phillips, Delbert R.

Chemistry of carbon compounds

Miscellaneous organic carbon compounds

C-metal

C07D23904

Patent

active

040585271

ABSTRACT:
N,N'-Dicarboxymethyl-1,3-propanediamine (designated PDDA) is prepared by reacting 1,3-propanediamine with formaldehyde and HCN to form hexahydropyrimidine-1,3-diacetonitrile, which is hydrolyzed with an aqueous alkali metal hydroxide to form dialkali metal hexahydropyrimidine-1,3-diacetate which, in turn, is reacted with mineral acid to form the desired PDDA and formaldehyde.
N,n'-dicarboxymethyl-2-hydroxy-1,3-propanediamine (designated HYDROXY-PDDA) is prepared by reacting 1,3-diamino-2-propanol with formaldehyde and HCN to form 5-hydroxyhexahydropyrimidine-1,3-diacetonitrile, which is hydrolyzed with an aqueous alkali metal hydroxide to form dialkali metal 5-hydroxyhexahydropyrimidine-1,3-diacetate which, in turn, is reacted with acid to form the desired HYDROXY-PDDA and formaldehyde.

REFERENCES:
brown et al., "The Pyrimidines", 1962, pp. 452-454.
Wagner et al., Syn. Org. Chem., pp. 412-414.

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