HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Diethyl Pyrocarbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Pyrocarbonate | HCID 15238643 | — |
| Reactant | Sodium ethyl carbonate | HCID 23677505 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl Pyrocarbonate | HCID 3051 | — |
| Product | Sodium Chloride | HCID 5234 | — |
Reaction Steps
The dialkyl pyrocarbonates may be prepared by reacting alkali metal alkyl carbonate, e.g., sodium ethyl carbonate, with alkyl halocarbonate, e.g., ethyl chlorocarbonate (ethyl chloroformate). The alkyl groups of the alkyl carbonate and halocarbonate are chosen to correspond to the alkyl group desired for the pyrocarbonate. For example, sodium ethoxide, which can be prepared by dissolving sodium metal in toluene solution of ethyl alcohol, is carbonated with carbon dioxide to prepare sodium ethyl carbonate. Thereafter, the sodium ethyl carbonate is reacted with ethyl chloroformate to form diethyl pyrocarbonate and sodium chloride. The chloride salt is filtered and the pyrocarbonate recovered by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05084529 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-e6af996c91c948b8bc00e2bf5be404ae |
| Source note | uspto-grants-1992_01 |