Amines cyclic proton transfer

The process for initiating radical formation in aromatic amine-vinyl monomer systems have been studied by Feng et al. [80-86] who proposed the formation of an aminium radical as the active state of an exciplex as intimate ion-pair and then a cyclic transition state which then would undergo a proton transfer process of deprotonation leading to the formation of active radical species for initiation as follows ... 

The reaction was found to be first order with respect to amines and acrylamides and no base catalysis was observed. The reaction is believed to occur in a single step in which the addition of amine to Cp of acrylamide and proton transfer from amine to Ca of acrylamide take place concurrently with a four-membered cyclic transition-state structure. The Hammett (px) and Brpnsted (/3X) coefficients are rather small, suggesting an early transition state (TS). The sign and magnitude of the cross-interaction constant, pxy(= —0.26), is comparable to those found in the bond formation processes in the. S n2 and addition reactions. The normal kinetic isotope effect ( h/ d > 1.0) and relatively low A and large negative Avalues are also consistent with the mechanism proposed.192... 

Mechanistic Studies. - A kinetic study of the solvolysis of the cyclic phosphoramidite (65) in methanol at 40 °C, catalysed by different amine hydrochlorides, showed that kcat obeyed the Bronsted equation with a = 0.65. This means that a proton transfer is well advanced in the TS, which was depicted as (66). Reactions of phosphoramidites with phenols are not catalysed by amine hydrochlorides and proceed sluggishly without a solvent aromatic solvents, e.g. 

Heteroaromatic aldehydes are excellent electrophiles in the MBH reaction because of their increased electrophilicity. The heteroatom also facilitates the proton transfers involved in the reaction (Scheme 1.53)/ In the presence of DABCO, pyridine-2-carboxaldehyde derivatives react rapidly with acrylates, methyl vinyl ketone and acrylonitrile to give excellent yields of the MBH adducts 112, which can be further transformed into indolizines 114 by thermal cyclization of their acetate derivatives 113 (Scheme 1.54)/ Notably, a small amount of indolizine 114 was formed along with normal MBH adduct 112 in the reaction of pyridine-2-carboxaldehyde with methyl vinyl ketone. Similarly, substituted 2-chloronicotin aldehydes 115 are reactive and efficient in the MBH reaction of methyl acrylates, acrylonitrile and cyclic enones catalyzed by various tertiary amine catalysts, such as DABCO, DBU, imidazole and 1-methylimidazole, to provide novel MBH adducts 116 and 117 for biological activity screening (Scheme 1.55). ... 

Kinetic studies of Michael addition of alicyclic secondary amines to ethyl propiolate in H2O and MeCN have demonstrated a substantial solvent effect on reactivity and transition-state structure. The amines were found to be less reactive in MeCN, although they are by 7-9 units more basic in the aprotic solvent. The reaction rates for morpholine and deuterated morpholine proved to be identical, which rules out both a stepwise mechanism in which proton transfer would occur in the RLS and a concerted mechanism in which nucleophilic attack and proton transfer would occur through a four-membered cyclic transition state. Consequently, a stepwise mechanism with proton transfer occurring after the RLS is probable. Br0nsted-type plots were found to be linear with = 0.29 and 0.51 in H2O and MeCN, respectively, indicating that bond formation is not advanced significantly in the RLS. The small value is also consistent with the absence of isotope effect. ... 

The amino group adds to the electrophilic carbon of the aldehyde function, and proton transfer generates an aminal elimination of water forms the corresponding imine. As a result of the proximity of the adjacent hydroxyl group, ring closure, followed by proton transfer, to form a cyclic oxazolidine will occur. 

The formation of 20 is basically a reaction in which a 1,2-dicarboxylic acid and a 1,2-diamine react to form a cyclic diamide or hydrazide. The mechanistic steps by which an acid and amine are converted to an amide are portrayed in Scheme 20.4. The acid and amine are in rapid equilibrium with the corresponding ammonium salt and the carboxylate ion, the latter of which is not subject to nucleophilic attack at the carbonyl carbon atom. The acid itself may undergo nucleophilic attack, however, so the small amount of it that exists at equilibrium (see Exercise 4) reacts with free amine to produce the tetrahedral zwitterionic intermediate 21. Subsequent proton transfers and loss of water afford the amide 22. Repetition of this series of steps generates 20. 

Tertiary amines like benzyldimethylamine, pyridine, and imidazole have been widely used as a base to initiate the anionic polymerization of PGE and its derivatives as well as for the synthesis of epoxy resins of diglycidyl ether of bisphenol A (DGEBA). Even if initiation occurs with amine alone, the introduction of an alcohol is a common procedure to suppress the observed induction period and increase the polymerization rate. Two initiation mechanisms have been proposed (Scheme 18) (1) direct nucleophilic attack of the amine onto the cyclic monomer to yield the zwitterion (a) and (2) formation of alkoxide (b) via proton transfer in the presence of alcohol. Fast exchange between dormant alcohol and active alkoxide allows chain growth from both initial amine (a) and alcohol (b). Poly(PGE) oligomers whose degree of polymerization does not exceed 5 are obtained. The presence of terminal double bonds indicates significant transfer to the monomer via... 

Enby 6 is an example of a stereospecific elimination reaction of an alkyl halide in which the transition state requires die proton and bromide ion that are lost to be in an anti orientation with respect to each odier. The diastereomeric threo- and e/ytAra-l-bromo-1,2-diphenyl-propanes undergo )3-elimination to produce stereoisomeric products. Enby 7 is an example of a pyrolytic elimination requiring a syn orientation of die proton that is removed and the nitrogen atom of the amine oxide group. The elimination proceeds through a cyclic transition state in which the proton is transferred to die oxygen of die amine oxide group. 

The electrochemistry of dioxoosmium(VI) complexes has also been extensively studied. The tra 5-dioxoosmium(VI) complexes of polypyridyl and macrocyclic tertiary amine ligands display very similar proton-coupled electron transfer couples. In aqueous solutions at pH < 5-7 the cyclic voltammograms of n-a i-[0s (0)2(bpy)2] show a remarkable reversible three-electron couple and a one-electron Os coimle. In the Pourbaix diagram two break points are observed in the pH dependence of the Os couple, which correspond to the pAa values of Os —OH2 and Os —(OHXOH2) (Figure 10). The redox reactions are shown in Equations (41)-(43). At pH >8 the 3e Os wave splits into a pH-independent le Os wave and a 2e/2H" Os wave (Equations (44) and (45)). 

According to the available experimental data, it is impossible to distinguish between these mechanisms, but the second mechanism seems to be preferred [Scheme (7)] for, according to this Scheme, the reaction of amine addition proceeding through a cyclic transition state is completed in one step, whereas for the reaction to occur according to Scheme (2) or (6) it is additionally necessary to transfer the proton. Then, it is probable that the different mechanisms [Schemes (3) and (5)] may precede formation of one and the same transition state [Scheme (7)]. Note finally that the mechanism of bifunctional catalysis [Scheme (7)] is extremely popular in different reactions of nucleophilic substitution at the saturated carbon atom and reactions with participation of a carbonyl group32>. 

Proton donors may be present or formed at the beginning of copolymerization and are necessary for the formation of primary active centres. In such a case, initiation according to Fischer s mechanism 39,40 (Eq. (37)) does not take place. Although the formation of a zwitterion (betaine-like structure) supports the possibility of the generation of charge-transfer complexes between cyclic anhydrides and amines, which may yield betaine-like structures82), simple anhydrides are much weaker ti acceptors than the often employed tetrachlorophthalic anhydride. 

PET activations of cyclic tertiary amines utilizing 1,4-dicyanonaphtha-lene (DCN) as electron acceptor have been studied by Pandey et al. [37]. The iminium cationic intermediates are generated via a electron-proton-electron (E-P-E) transfer sequence in a highly regiospecific fashion and as an example, tetrahydro-l,3-oxazines (26) were synthesized from substrates 25 with high control of regio- and stereoselectivity (Sch. 16). 

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