Carbonate ester

Revision as of 15:19, 4 September 2012 by WikiBot (talk | contribs) (Robot: Automated text replacement (-{{WikiDoc Cardiology Network Infobox}} +, -<references /> +{{reflist|2}}, -{{reflist}} +{{reflist|2}}))
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
File:Carbonate ester.png
Chemical structure of the carbonate ester group.

A carbonate ester is a functional group in organic chemistry consisting of a carbonyl group flanked by two alkoxy groups. The general structure of these carbonates is R1O(C=O)OR2 and they are related to esters R1O(C=O)R and ethers R1OR2 and also to the inorganic carbonates.

Carbonate esters are used as protecting group for diols. A classic reagent is phosgene but more user friendly reagents exist such as carbonyl diimidazole. Ethylene carbonate and Propylene carbonate are used as a solvent. Dimethyl carbonate is used as a methylating reagent.

In many applications a carbonate group replaces an ester group for example in Cholesteryl oleyl carbonate. Polycarbonates are an important class of polymers.

Organic synthesis

Laboratory methods for the synthesis of carbonate ester in the laboratory are:


  1. Zinc(II)-pyridine-2-carboxylate / 1-methyl-imidazole: a binary catalytic system for in the synthesis of cyclic carbonates from carbon dioxide and epoxides Arkivoc 2007 (iii) 151-163 (EA-2262DP) Thomas A. Zevaco, Annette Janssen, and Eckhard Dinjus Link