145147-70-2

Basic information

• Product Name: N,N-dibenzylalanine
• CAS NO: 145147-70-2
• Molecular Weight: 269.343
• Mol File: 145147-70-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N-dibenzylalanine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dibenzylalanine(145147-70-2)
• EPA Substance Registry System: N,N-dibenzylalanine(145147-70-2)

Safety Data

• Hazardous Substances Data: 145147-70-2(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 302-72-7 rac-Ala-OH 
• 100-39-0 benzyl bromide 

Downstream Products

• 116031-73-3 N,N-dibenzyl-alanyl=>tryptophyl=>2-amino-butyric acid ethyl ester 
• 103280-10-0 N^α-(N,N-Dibenzyl-alanyl)-tryptophan 
• 145147-74-6 (2S^*,3S^*,4R^*)-2-(Dibenzylamino)-3,4-diphenyl-3-pentanol 
• 145147-74-6 (2S^*,3S^*,4S^*)-2-(Dibenzylamino)-3,4-diphenyl-3-pentanol 
• 145147-72-4 (2S^*,4R^*)-2-(Dibenzylamino)-4-phenyl-3-pentanone 
• 145147-72-4 (2S^*,4S^*)-2-(Dibenzylamino)-4-phenyl-3-pentanone 
• 145147-71-3 2-(Dibenzylamino)-N-methoxy-N-methylpropionamide 
• 80993-76-6 2-(Dibenzylamino)-1-phenyl-1-propanone 
• 112302-87-1 2-dibenzylaminopropionic acid methyl ester 
• 93406-80-5 (S)-α-(N,N-dibenzylamino)propanoic acid 
• 188798-85-8 (R)-2-(N,N-dibenzylamino)propanoic acid 
• 103209-64-9 N^α-(N,N-dibenzyl-alanyl)-tryptophan-methyl ester 

Relevant articles and documents

Resolution of racemic N-benzyl α-amino acids by liquid-liquid extraction: A practical method using a lipophilic chiral cobalt(III) salen complex and mechanistic studies

The efficient resolution of racemic N-benzyl α-amino acids (N-Bn-AA) has been achieved by a liquid-liquid extraction process using the lipophilic chiral salen-cobalt(III) complex [CoIII(3)(OAc)]. As a result of the resolution by extraction, one enantiomer (S) of the N-benzyl α-amino acid predominated in the aqueous phase, while the other enantiomer (R) was driven into the organic phase by complexation to cobalt. The complexed amino acid (R) was then quantitatively released by a reductive (CoIII→Co II) counter-extraction with aqueous sodium dithionite or L-ascorbic acid in methanol. The reductive cleavage allowed to recover the [Co II(3)] complex in good yield, which could be easily re-oxidized to [CoIII(3)(OAc)] with air/AcOH and reused with essentially no loss of reactivity and selectivity. Investigation on the nitrogen substitution indicates that the presence of a single benzyl group on the amino acid nitrogen is important to obtain high enantioselectivity in the extraction process. The kinetic vs. thermodynamic nature of the resolution process was also investigated with an enantiomeric exchange experiment, which shows that the liquid-liquid extraction with [CoIII(3)-(OAc)] is an equilibrium process operating under thermodynamic control. In the absence of a suitable crystal structure of the [CoIII(3)(N-Bn-AA)] complexes, computational and spectroscopic studies were used to investigate how the N-benzyl α-amino acids are accommodated in the "binding pocket" of the chiral cobalt complex. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

On the Configurational Stability of α-Methylbenzyllithium

α-Methylbenzyllithium (6) should possess either central or planar chirality.The rate of enantiomerization of 6 at -78 deg C was found to be faster than its addition to the amide 7, the ketone 8, or to the aldegyde 10, according to a test based on kinetic