Catalyst-Assisted Selective Vinylation and Methylallylation of a Quaternary Carbon Center Using tert-Butyl Acetate

The In(OTf)₃-catalyzed α-vinylation of various hydroxy-functionalized quaternary carbon centers using in situ generated isobutylene from tert-butyl acetate is presented as a novel synthetic methodology. Moreover, tert-butyl acetate is a nonflammable feed stock and is a readily available source for the in situ production of vinyl substituents, as demonstrated by the vinylation reaction with quaternary hydroxy/methoxy compounds. Moreover, an excellent selectivity for methylallylation over vinylation was obtained with Ni(OTf)₂ as a catalyst. In the case of peroxyoxindole, methylallyl-functionalized 1,4-benzoxazin-3-one derivatives were formed through the sequential rearrangement of peroxyoxindole followed by the nucleophilic attack by isobutylene. The detailed mechanism for this reaction and rationalization for the selectivity are provided using kinetics and density functional theory studies.