Aromatic C-H insertion of β-phenoxyalkylidenecarbenes generated by reaction of alkynyl(p-phenylene)bisiodonium ditrifluoro-methanesulfonates (ditriflates) with phenoxide anions
Reaction of alkynyl(p-phenylene)bisiodonium ditriflates with sodium phenoxide in methanol provides 2-substituted benzofurans in 49-62% yields. This result indicates that β-phenoxyalkylidenecarbenes are generated by the reaction with phenoxide anion and undergo novel intramolecular aromatic C-H insertion to afford benzofurans. 2-Phenoxy-2-phenylethenylidene generated analogously in situ underwent competing processes of aromatic C-H insertion and 1,2-phenyl migration. The corresponding reactions with 4-substituted phenoxide ions also afforded 5-substituted benzofurans and, as the minor products, 2-aryloxy-1-iodoalk-1-enes which were probably derived from the intermediate vinyliodonium salts. Reactions of alkynyl(p-phenylene)bisiodonium ditriflates with sodium [2H5]phenoxide (98% 2H) in methanol gave deuterated 2-alkylbenzofurans in 35-40% yields and the hydrogen at the 3-position of the benzofurans was deuterated completely. This result strongly supports selective aromatic C-H insertion of the in situ generated β-phenoxyalkylidenecarbenes.
A Versatile Two-Stage Synthesis of 2-Substituted Benzofurans from (2-Methoxyphenyl)ethynes
(2-Methoxyphenyl)ethynes react with aryl or alkyl halides to give disubstituted alkynes which are converted into the corresponding 2-substituted benzofurans on treatment with lithium iodide in 2,4,6-trimethylpyridine.
Buckle, Derek, R.,Rockell, Caroline J. M.
p. 2443 - 2446
(2007/10/02)
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