2015•Chemistry LettersRequires access

Pummerer Reaction of Sulfoxides in Acetic Anhydride Catalyzed by Al-MCM-41

Suguru Ito, Yoshihiro Kubota, Masatoshi Asami

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Abstract

The Pummerer reaction of acetic anhydride with both alkyl aryl sulfoxides and dialkyl sulfoxides was efficiently promoted by a mesoporous aluminosilicate Al-MCM-41 to afford the corresponding α-acetoxy sulfides in high yields. The catalyst was easily recovered by filtration and could be reused three times without a significant loss of catalytic activity.

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What this paper is about

The Pummerer reaction of acetic anhydride with both alkyl aryl sulfoxides and dialkyl sulfoxides was efficiently promoted by a mesoporous aluminosilicate Al-MCM-41 to afford the corresponding α-acetoxy sulfides in high yields. The catalyst was easily recovered by filtration and could be reused three times without a significant loss of catalytic activity.

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Available abstract

The Pummerer reaction of acetic anhydride with both alkyl aryl sulfoxides and dialkyl sulfoxides was efficiently promoted by a mesoporous aluminosilicate Al-MCM-41 to afford the corresponding α-acetoxy sulfides in high yields. The catalyst was easily recovered by filtration and could be reused three times without a significant loss of catalytic activity.

Key concepts: Pummerer rearrangement, Acetic anhydride, Chemistry, Catalysis, Aryl, Filtration (mathematics), Alkyl, Aluminosilicate

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