Mechanistic evaluation of the halocyclization of 4-penten-1-ol by some bis(2-substituted pyridine) and bis(2,6-disubstituted pyridine)bromonium triflates

The halocyclization reaction of 4-penten-1-ol mediated by various bis(2-sub stituted pyridine) and (2,6-disubstituted pyridine)bromonium triflates (P2B r+OTf-) was investigated to determine the influence of the substituents on the mechanism of reaction. In all cases, the reaction proceeds via a two-st ep process where the starting P2Br+ reversibly dissociates to a reactive mo nosubstituted PBr+, which then is captured by 4-penten-1-ol to form halocyc lized product (2-bromomethyltetrahydrofuran). The dissociation rate constan t of P2Br+ (k(d)) is sensitive to the steric bulk at the 2- and 6-positions , and in the case of the 2,6-dicyclohexylpyridine or 2,6-dicyclopentylpyrid ine, the P2Br+ species are too unstable to isolate. The partitioning ratio of the reactive intermediate (PBr+) between reversal and product formation (k(-d)/k(2)) is not particularly sensitive to the nature of the pyridine, t he limiting values being 3-7 except in the case of bis(2(-)-menthylpyridine )bromonium triflate where the k(-d)/k(2) ratio is similar to 80. The reacti on of 4-penten-1-ol and its OD isotopomer with bis(lutidine)bromonium trifl ate was investigated to determine the deuterium kinetic isotope effect (dki e) on the bromocyclization reaction. The (k(-d)/k(2))(H/D) ratio is 1.0, in dicating that the rate-limiting step for the bromocyclization is probably f ormation of a PBr+-4-penten-1-ol complex which does not involve substantial changes in the bonding of the OH. The cyclization of 4-penten-1-ol and 4-p entenoic acid mediated by bis(2(-)-menthylpyridine)bromonium triflate produ ces an enantiomeric excess in the cyclized products of only 2.4% and 4.8% r espectively.