Carbon Dioxide → trans-Aconitic acid

HRID 1707132Notes

Reaction equation

HRID 1707132 reaction equation
[C:1](C([O-])=O)([C:10]([O-:12])=[O:11])=[C:2]([C:7]([O-:9])=[O:8])[CH2:3][C:4]([O-:6])=[O:5].[Na+].[Na+].[Na+].[Na+].Cl.C(=O)=O>O>[CH2:3]([C:4]([OH:6])=[O:5])/[C:2](/[C:7]([OH:9])=[O:8])=[CH:1]\[C:10]([OH:12])=[O:11]

Participants

5

Reactant 3

HCID 280Carbon DioxideHCID 313Hydrochloric AcidHCID 20558963HCID 20558963, compound

Product 1

HCID 444212trans-Aconitic acid

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

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##

Workup

  1. customThe residue, after evaporation of water
  2. extractionis extracted with acetone
  3. customThe acetone is evaporated
  4. customto leave a residue

Sources & evidence

ORD record
ord-5baa9e56896d441a9d4700350ebc3def
Source dataset
uspto-grants-1980_06
Patent number
US04209636

Reaction notes

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