Making tertiary amines and their salts
المؤلف:
University of Missouri System
المصدر:
Organic Chemistry ii
الجزء والصفحة:
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27-10-2020
1739
Making tertiary amines and their salts
But it doesn’t stop here! The diethylamine also reacts with bromoethane – in the same two stages as before. This is where the reaction would start if you reacted a secondary amine with a halogenoalkane.
In the first stage, you get triethylammonium bromide.
There is again the possibility of a reversible reaction between this salt and excess ethylamine in the mixture.
The ethylamine removes a hydrogen ion from the triethylammonium ion to leave a tertiary amine – triethylamine.
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