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Testing how much trisubstituted amines can bulk up

Using a multitude of methods, chemists make unprecedented crowded alkyl amines; but one elusive target remains out of reach

by Tien Nguyen
April 30, 2018

Researchers made tertiary amines with tremendous steric congestion (left). But tri-tert-butylamine, arguably the most crowded alkylamine, resisted all synthetic attempts.

By nature, nitrogen prefers to bond with three molecular companions. But, when it comes to bulky alkyl groups, amines are choosy about the company they keep and have resisted many chemists’ campaigns to form highly hindered tertiary amines. This class of alkylamines, though, has been useful in many applications, including as precursors to photostabilizers and polymerization inhibitors and as reagents in catalysis since their bulk blocks them from binding and deactivating catalysts.

Now a team led by Klaus Banert at the Chemnitz University of Technology has attempted to determine how much steric stress these compounds can tolerate. Using 10 previously reported approaches, they synthesized more than a dozen alkylamines that they claim have unprecedented steric crowding (J. Org. Chem. 2018, DOI: 10.1021/acs.joc.8b00496).

The researchers observed that the main obstacle to making the hindered amines was their tendency to undergo Hofmann-like elimination reactions. In this type of reaction, the nitrogen plucks a hydrogen off a neighboring carbon to kick off one of the alkyl group substituents, leaving behind an alkene and a less bulky disubstituted amine. The group proposed that while tert-butyl substituted amines were particularly susceptible to this degradation pathway, the arguably larger adamantyl groups would be immune to such elimination given the orientation of its pluckable hydrogens.

The team confirmed the synthesis of the highly hindered amines, including those with adamantyl groups, using nuclear magnetic resonance spectroscopy. Surprisingly, the researchers detected distinct NMR peaks for protons on identical alkyl groups around the congested amines, indicating that rotation of the substituents was restricted due to the sterics.

However, despite numerous attempts, the authors were unable to make tri-tert-butylamine, one of the most hindered of tertiary amines. “I had to distribute the attempts among several coworkers to minimize frustration,” Banert says. He and his colleagues question whether anyone will ever isolate the compound at room temperature. Chemists have long debated this idea.

Twenty-two years ago, Armin de Meijere, professor emeritus at University of Göttingen, and colleagues made di-tert-butylcyclopropylamine, previously thought to be one of the most hindered tertiary amines isolable at room temperature. He thinks that the new work pushes the limits of sterically congested amines forward considerably, but agrees that the elusive tri-tert-butylamine will probably never be made.

Peter R. Schreiner of Justus Liebig University Giessen is more optimistic, albeit with caveats. “I am not fully convinced that tri-tert-butylamine, or even more so tri-adamantylamine, cannot be made, though perhaps only at very low temperatures,” Schreiner says. He points out that tri-adamantylphosphine has recently been reported (J. Am. Chem. Soc. 2016, DOI: 10.1021/jacs.6b03215), which suggests that there could be hope for the nitrogen equivalent. But because C–N bonds are shorter than C–P bonds, tri-tert-butylamine will probably take more effort, he says.


Peter Livant, who was at Auburn University and is now retired, also thinks tri-tert-butylamine may one day show itself, but whether it’s stable for one second or 20 years is unknown.

“What struck me about this article is that they were after a sort of Holy Grail. They wanted to reach the top of a mountain that’s never been scaled before,” Livant says. “That sense of adventure was really nice.”



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Paul E. Eckler (May 2, 2018 3:15 PM)
I surprised this article failed to mention DABCO. It's a powerful urethane foam catalyst and commercially available.
A. Chandrasekaran (May 2, 2018 10:08 PM)
But, in terms of steric factor, DABCO is less than triethylamine (TEA). As of I know & use, Hunig's base (DiisopropylEthylAmine, DIPEA) is the bulkiest amine with large scale commercial availability.
A. Anderson (May 6, 2018 9:28 PM)
About 30 years ago, F. Marsh and I (DuPont CRD) tried a double displacement reaction on N,N-dichloro-tert-butylamine with t-butyllithium. The reaction was quite exothermic and required strong cooling. We attempted to isolate the amine by acid and base extraction. A MS spectrum appeared to support tri-t-butylamine. The yield was poor. Management was not enthused. So we elected to drop the project. If I were to try it again, I would choose to start with N-chloro-di-tertbutylamine to cut down on the exothermic nature of the displacement.
Prof. Dr. Klaus Banert (September 19, 2018 7:20 AM)
Klaus Banert
We performed the suggested reaction of N-chloro-di-tert-butylamine several times in 2017 by using tert-butyllithium from different suppliers. Indeed, we obtained, in very low yield (about 1%), a product with the right mass (GC-MS) and suitable retention time (GC). Moreover, the crude substance showed a strong signal of a tert-butyl group in 1H and 13C NMR spectra. After purification, however, it turned out that the structure of this product was n-butyl-di-tert-butylamine, which can be prepared from the same N-chloro compound and n-butyllithium in high yield. Possibly, buyable tert-butyllithium includes a small impurity of n-butyllithium.

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