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In organic chemistry, a carbonate ester (organic carbonate or organocarbonate) is an ester of carbonic acid. This functional group consists of a carbonyl group flanked by two alkoxy groups. The general structure of these carbonates is R−O−C(=O)−O−R' and they are related to esters (R−O−C(=O)−R'), ethers (R−O−R') and also to the inorganic carbonates.
Monomers of polycarbonate (e.g. Makrolon or Lexan) are linked by carbonate groups. These polycarbonates are used in eyeglass lenses, compact discs, and bulletproof glass. Small carbonate esters like dimethyl carbonate, ethylene carbonate, propylene carbonate are used as solvents, dimethyl carbonate is also a mild methylating agent.
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Carbonate esters have planar OC(OC)2 cores, which confers rigidity. The unique O=C bond is short (1.173 Å in the depicted example), while the C-O bonds are more ether-like (the bond distances of 1.326 Å for the example depicted).[1]
Carbonate esters can be divided into three structural classes: acyclic, cyclic, and polymeric. The first and general case is the acyclic carbonate group. Organic substituents can be identical or not. Both aliphatic or aromatic substituents are known, they are called dialkyl or diaryl carbonates, respectively. The simplest members of these classes are dimethyl carbonate and diphenyl carbonate.
Alternatively, the carbonate groups can be linked by a 2- or 3-carbon bridge, forming cyclic compounds such as ethylene carbonate and trimethylene carbonate. The bridging compound can also have substituents, e.g. CH3 for propylene carbonate. Instead of terminal alkyl or aryl groups, two carbonate groups can be linked by an aliphatic or aromatic bifunctional group.
A third family of carbonates are the polymers, such as poly(propylene carbonate) and poly(bisphenol A carbonate) (e.g. Makrolon or Lexan).
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Organic carbonates are not prepared from inorganic carbonate salts.[citation needed] Two main routes to carbonate esters are practiced: the reaction of an alcohol (or phenol) with phosgene (phosgenation), and the reaction of an alcohol with carbon monoxide and an oxidizer (oxidative carbonylation). Other carbonate esters may subsequently be prepared by transesterification.[2][3]
In principle carbonate esters can be prepared by direct condensation of methanol and carbon dioxide. The reaction is however thermodynamically unfavorable.[4] A selective membrane can be used to separate the water from the reaction mixture and increase the yield.[5][6][7][8]
Diphenyl carbonate, a representative acyclic carbonate ester
Dimethyl dicarbonate, a preservative
Ethylene carbonate, a cyclic carbonate ester
Trimethylene carbonate, another cyclic carbonate ester
Poly(bisphenol A carbonate), a commercially important plastic (Lexan)
Phosgenation
Alcohols react with phosgene to yield carbonate esters according to the following reaction:
- 2 ROH + COCl2 → ROC(O)OR + 2 HCl
Phenols react similarly. Polycarbonate derived from bisphenol A is produced in this manner. This process is high yielding. However, toxic phosgene is used, and stoichiometric quantities of base (e.g. pyridine) are required to neutralize the hydrogen chloride that is cogenerated.[2][3] Chloroformate esters are intermediates in this process. Rather than reacting with additional alcohol, they may disproportionate to give the desired carbonate diesters and one equivalent of phosgene:[3]
- PhOH + COCl2 → PhOC(O)Cl + HCl
- 2 PhOC(O)Cl → PhOC(O)OPh + COCl2
Overall reaction is:
- 2 PhOH + COCl2 → PhOC(O)OPh + 2 HCl
Oxidative carbonylation
Oxidative carbonylation is an alternative to phosgenation. The advantage is the avoidance of phosgene. Using copper catalysts, dimethylcarbonate is prepared in this way:[3][9]
- 2 MeOH + CO + 1/2 O2 → MeOC(O)OMe + H2O
Diphenyl carbonate is also prepared similarly, but using palladium catalysts. The Pd-catalyzed process requires a cocatalyst to reconvert the Pd(0) to Pd(II). Manganese(III) acetylacetonate has been used commercially.[10]
Reaction of carbon dioxide with epoxides
The reaction of carbon dioxide with epoxides is a general route to the preparation of cyclic 5-membered carbonates. Annual production of cyclic carbonates was estimated at 100,000 tonnes per year in 2010.[11] Industrially, ethylene and propylene oxides readily react with carbon dioxide to give ethylene and propylene carbonates (with an appropriate catalyst).[2][3] For example:
- C2H4O + CO2 → C2H4O2CO
Carbonate transesterification
Carbonate esters can be converted to other carbonates by transesterification. A more nucleophilic alcohol will displace a less nucleophilic alcohol. In other words, aliphatic alcohols will displace phenols from aryl carbonates. If the departing alcohol is more volatile, the equilibrium may be driven by distilling that off.[2][3]
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Carbonate esters undergo many of the reactions of conventional carboxylic acid esters. With Grignard reagents carbonate esters react to give tertiary alcohols. Some cyclic carbonates are susceptible to polymerization.
Organic carbonates are used as solvents in lithium batteries. Due to their high polarity, they dissolve lithium salts. The problem of high viscosity is circumvented by using mixtures for example of dimethyl carbonate, diethyl carbonate, and dimethoxyethane.
They are also used as solvents in organic synthesis.[12] Classified as polar solvents, they have a wide liquid temperature range. One example is propylene carbonate with melting point −55 °C and boiling point 240 °C. Other advantages are low ecotoxicity and good biodegradability. Many industrial production pathways for carbonates are not green because they rely on phosgene or propylene oxide.[13]
Dimethyl dicarbonate is commonly used as a beverage preservative, processing aid, or sterilant.[14]
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