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Catalytic oxidative cleavage of catechol by a non-heme iron(iii) complex as a green route to dimethyl adipate†
Robin Jastrzebski,Bert M. Weckhuysen,Pieter C. A. Bruijnincx
Chemical Communications Pub Date : 06/26/2013 00:00:00 , DOI:10.1039/C3CC42423E
Abstract

The catalyst system prepared in situ from iron(III) salts, tris(2-pyridylmethyl)amine and a base readily catalyses the intradiol dioxygenation of pyrocatechol in methanol, to primarily afford the half-methyl ester of muconic acid. Dimethyl adipate is obtained by the subsequent, one-step catalytic hydrogenation/esterification, thus providing a green route to this important nylon precursor.

Graphical abstract: Catalytic oxidative cleavage of catechol by a non-heme iron(iii) complex as a green route to dimethyl adipate
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