Manganese Catalysed Dehydrogenative Synthesis of Urea Derivatives and Polyureas

29 December 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Urea derivatives are prevalent intermediates in the synthesis of resin precursors, dyes, agrochemicals, and pharmaceutical drugs. Furthermore, polyureas are useful plastics with applications in coating, adhesive, and biomedical industries and have a current annual market of USD 885 million. However, the conventional methods for the synthesis of urea derivatives and polyureas involve toxic reagents such as (di)isocyanates, phosgene, CO, and azides. We present here the synthesis of (poly)ureas using much less toxic reagents - (di)amines, and methanol via a catalytic dehydrogenative coupling process. The reaction is catalyzed by a pincer complex of an earth-abundant metal, manganese, and liberates H2 gas, valuable by itself, as the only by-product making the overall process atom-economic, and sustainable. A broad variety of symmetrical, and unsymmetrical urea derivatives and polyureas have been synthesized in moderate to quantitative yields using this catalytic protocol. Mechanistic insights have also been provided using experiments and DFT computation suggesting that the reaction proceeds via an isocyanate intermediate.

Keywords

Catalysis
Dehydrogenation
Manganese
Methanol
Pincer
Polyurea
Urea

Supplementary materials

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Description
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Supporting information
Description
Supporting information contains details of catalytic dehydrogenation, synthesis/characterization of (poly)ureas, mechanistic studies, NMR, IR, MALDI-TOF mass spectrometry and computational details.
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