Autocatalytic Oxidation of Ethers with Sodium Bromate
Date
2012-11-21
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Abstract
Sodium and potassium bromate are stable and easily stored oxidants. They can oxidize both open and cyclic ethers in aqueous
solution at room temperature yielding esters and lactones. Kinetic studies of the oxidation of tetrahydrofuran to g-butyrolactone indicate that
the major active oxidation species is bromine and not bromate. The bromate is only a supporting agent, responsible for the initiation step and
supplying bromine molecules by oxidizing bromide ions during the propagation step. In the oxidation of tetrahydrofuran, high yields of
g-butyrolactone were obtained. q2000 Elsevier Science Ltd. All rights reserved.
Description
Sodium and potassium bromate are stable and easily stored oxidants. They can oxidize both open and cyclic ethers in aqueous
solution at room temperature yielding esters and lactones. Kinetic studies of the oxidation of tetrahydrofuran to g-butyrolactone indicate that
the major active oxidation species is bromine and not bromate. The bromate is only a supporting agent, responsible for the initiation step and
supplying bromine molecules by oxidizing bromide ions during the propagation step. In the oxidation of tetrahydrofuran, high yields of
g-butyrolactone were obtained. q2000 Elsevier Science Ltd. All rights reserved.
Keywords
Autocatalytic Oxidation of Ethers with Sodium Bromate
