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July 1, 2001Pure and Applied Chemistry160 citationsOpen Access

New developments in dimethyl carbonate chemistry

PTPietro Tundo

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Abstract

Dimethylcarbonate (DMC) is a valuable methylating reagent which can replace methyl halides and dimethylsulfate in the methylation of a variety of nucleophiles. It couples tunable reactivity and unprecedented selectivity toward mono-C- and mono-N-methylation in the reactions of acidic CH2 and primary aromatic amines, respectively. In addition, it is a prototype example of a green reagent, since it is nontoxic, made by a clean process, and biodegradable, and it reacts in the presence of a catalytic amount of base thereby avoiding the formation of undesirable inorganic salts as by-products. Other remarkable reactions are those where DMC behaves as an oxidant: cyclic ketones are transformed into a,w-dimethyl esters with a reaction of atom efficiency of 1.0.

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Pietro Tundo (2001) studied this question.

synapsesocial.com/papers/6a6594c5b94356a0f3337b16https://doi.org/10.1351/pac200173071117
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