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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616043Generated: October 29, 2026

Carbon Dioxide → HCID 86735439, compound

https://huagongshe.com/reaction/616043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
Reactant1,1,2,2-Tetraethyl 1,1,2,2-ethanetetracarboxylateHCID 79090—
ReactantSodium BromideHCID 253881—
CatalystTetraethylammonium BromideHCID 6285—
ProductHCID 86735439HCID 86735439—

Reaction Steps

It will be noted that when sodium iodide, which is soluble in acetonitrile without added crown ether, is employed instead of the mixture of tetraethylammonium bromide and sodium bromide, only one of the anionic sites in substantially all the tetraethyl ethane-1,1,2,2-tetracarboxylate dianion is utilized for proton abstraction. Thus one of the anionic sites is available for reaction with carbon dioxide to yield the sodium tetraethyl ethane-1,1,1,2,2-pentacarboxylate, which precipitates in the catholyte along with the disodium 4-methyl-3,5-dioxo-6H,1,4-oxazine-2,O3 -dicarboxylate. The mixture is readily separated, however, by treatment with water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072583
Source datasetuspto-grants-1978_02
ORD IDord-cc774fbcdd1b40858bbe06cb587b53c3
Source noteuspto-grants-1978_02