Nitrosation Chemistry of Pyrroline, 2-Imidazoline, and 2-Oxazoline: Theoretical Curtin-Hammett Analysis of Retro-Ene and Solvent-Assisted C-X Cleavage Reactions of α-Hydroxy-N-nitrosamines
The results are presented of a theoretical study of the nitrosation chemistry of pyrroline 1 (X = CH2), imidazoline 2 (X = NH), and 2-oxazoline 3 (X = O). Imines 1-3 are converted to the α-hydroxy-N- nitrosamines 7-9 via the N-nitrosoiminium ions 4-6. The NN-cis isomers of 7-9 may undergo retro-ene reactions to the δ-oxoalkyl diazotic acids 10-12. With the opportunity for microsolvation, C-X cleavage becomes possible for 8 and 9 and leads to the formation of N-(2-aminoethyl)- and N-(2-hydroxyethyl)-N- nitrosoformamides 15 and 16, respectively. The NN-isomerization barriers are comparable to the barriers for the ring-opening reactions, and the consideration of two Curtin-Hammett scenarios is required: CH-I for the NN-trans-rotamers of 7-9 to undergo C-X cleavage or NN-isomerization and CH-II for the NN-cis-rotamers to undergo C-X cleavage, C-N cleavage, or NN-isomerization. We determined all stereoisomers of the substrates, the products, and of all transition states structures for the retro-ene reactions of 7-9, the C-X cleavages of microsolvated 8 and 9, and the NN-isomerizations of 8 and 9. The potential energy surfaces were explored at the B3LYP/6-31G** level, and the results are discussed with emphasis on the comparison of the kinetics and thermodynamics of C-N versus C-X cleavage. The study shows all decompositions to be very fast with activation barriers below 21 kcal·mol-1, and the comparitive analysis predicts that the chemical toxicologies of 1 and 3 should be similar and remarkably different from that of 2.
H. Wu et al., "Nitrosation Chemistry of Pyrroline, 2-Imidazoline, and 2-Oxazoline: Theoretical Curtin-Hammett Analysis of Retro-Ene and Solvent-Assisted C-X Cleavage Reactions of α-Hydroxy-N-nitrosamines," Journal of Organic Chemistry, vol. 70, no. 17, pp. 6790-6801, American Chemical Society (ACS), Jul 2005.
The definitive version is available at https://doi.org/10.1021/jo050856s
Keywords and Phrases
Aromatic compounds; Chemical bonds; Isomerization; Reaction kinetics; Stereochemistry; Thermodynamics; Toxicity; Microsolvation; Nitrosation chemistry; Ring-opening reactions; Stereoisomers; Nitrogen compounds; 2 imidazoline derivative; nitrosamine; oxazoline derivative; pyrroline derivative; analytic method; chemical analysis; chemical reaction; comparative study; decomposition; isomerization; nitrosation; phase transition; reaction analysis; solvation; structure analysis; Hydrolysis; Imidazoles; Nitrosamines; Nitrosation; Oxazoles; Pyrroles; Solvents
International Standard Serial Number (ISSN)
Article - Journal
© 2005 American Chemical Society (ACS), All rights reserved.
01 Jul 2005