A photochemical retro-Friedel-Crafts alkylation. Rapid rearrangement of cyclohexadienyl cations

Article abstract of DOI:10.1139/v96-282

This paper reports the use of laser flash photolysis (LFP) techniques to show that cyclohexadienyl cations (σ complexes) of the Friedel-Crafts reaction of 1,3-dimethoxybenzene and the diphenylmethyl cation rearrange on the ns time scale without separating the aromatic compound and the electrophile. This is demonstrated through a study of the photochemical behaviour of 2-diphenylmethyl-1,3-dimethoxybenzene (4) in 1,1,1,3,3,3-hexafluoroisopropyl alcohol (HFIP). Derivatives of 1,3-dimethoxybenzene have previously been found to selectively protonate at C2 upon excitation in HFIP, and indeed the principal products with 4 are 1,3-dimethoxybenzene (6) and Ph₂CHOCH(CF₃)₂ (7), the species expected if the cyclohexadienyl cation formed in the C2 protonation cleaved Ph₂CH⁺. These products are, however, accompanied by 4-diphenylmethyl-1,3-dimethoxybenzene (8), a rearranged isomer of 4. A portion of this product is explained by the combination of Ph₂CH⁺ and 1,3-dimethoxybenzene as the latter accumulates during the irradiation. However, 11.5% of 8 is also seen upon extrapolation to zero time. LFP experiments on the ps time scale reveal that the C2 protonated cation, the 1-diphenylmethy 1-2,6-dimethoxybenzenium ion (5), is formed within 100-200 ps, and reacts with k = 9 × 10⁸ s^-1, with absorbance for Ph₂CH⁺ growing in as 5 decays. LFP studies on the ns time scale reveal that there is a second quantity of Ph₂CH⁺ that grows in, with k = 5.0 × 10⁵ s^-1. The precursor for this has been identified as the 1-diphenylmethyl-2,4-dimethoxybenzenium ion (10), the thermodynamically more stable isomer of 5. A mechanistic model is proposed in which excited 4 is C2 protonated in HFIP with k ≥ 1 × 10¹⁰ s^-1 to form 5, which loses Ph₂CH⁺ with k = 3 × 10⁸ s^-1 in competition with rearrangement to 10 with k = 6 × 10⁸ s^-1. The cation 10 serves as the second source of Ph₂CH⁺, losing Ph₂CH⁺ with k = 4 × 10⁵ s^-1; in competition 10 is deprotonated by HFIP to give 8 with k = 8 × 10⁴ s^-1. The 11.5% of the rearranged 8 that is observed at zero conversion is thus shown to come from an intramolecular pathway in which the key step is the migration of a diphenylmethyl group without separation: 4 → 4* → 5 → 10 → 8.