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I'm wondering if N,N dichloro butanediamine can be easily hydrolysed by say a strong base like NaOH.
Reason asking as 1, 4 butandiol was originally made by hydrolysing N, N dinitro-1,4-butanediamine, and I figure the chloro version would also yield 1, 4 butanediol.
Reason asking as 1, 4 butandiol was originally made by hydrolysing N, N dinitro-1,4-butanediamine, and I figure the chloro version would also yield 1, 4 butanediol.