HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → trans-Aconitic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20558963 | HCID 20558963 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans-Aconitic acid | HCID 444212 | — |
Reaction Steps
Nine grams of the product as prepared in Example XXIII, i.e. tetrasodium propene-1,1,2,3-tetracarboxylate, is dissolved in 10 mls water and acidified with dilute HCl (10%). Liberation of CO2 is instantaneous. The residue, after evaporation of water, is extracted with acetone. The acetone is evaporated to leave a residue consisting of a 1:1 by weight mixture of cis-trans aconitic acid. The structure of the product is confirmed by NMR analysis (D2O): ##STR73##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04209636 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-5baa9e56896d441a9d4700350ebc3def |
| Source note | uspto-grants-1980_06 |