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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5749Generated: October 24, 2026

Carbon Dioxide → Diethyl Pyrocarbonate

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantEthyl chloroformateHCID 10928—
ReactantCarbonate IonHCID 19660—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantPyrocarbonateHCID 15238643—
ReactantSodium ethyl carbonateHCID 23677505—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductDiethyl PyrocarbonateHCID 3051—
ProductSodium ChlorideHCID 5234—

Reaction Steps

The organic pyrocarbonates may be prepared by reacting alkali metal organic carbonate, e.g., sodium ethyl carbonate, with organic halocarbonate, e.g., ethyl chlorocarbonate (ethyl chloroformate). The organo groups of the organic carbonate and halocarbonate are chosen to correspond to the organo groups desired for the pyrocarbonate. For example, sodium ethoxide, which can be prepared by dissolving sodium metal in a 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246630
Source datasetuspto-grants-1993_09
ORD IDord-c92cfeae8c76411db9a7c282c6b1f728
Source noteuspto-grants-1993_09