HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 86735439, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,1,2,2-Tetraethyl 1,1,2,2-ethanetetracarboxylate | HCID 79090 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Catalyst | Tetraethylammonium Bromide | HCID 6285 | — |
| Product | HCID 86735439 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072583 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-cc774fbcdd1b40858bbe06cb587b53c3 |
| Source note | uspto-grants-1978_02 |