HCID 20390520, compound → 2-(Carboxymethoxy)butanedioic acid
Reaction equation
O.O.O.O.O.[C:6]([CH2:9][O:10][CH:11]([CH2:15][C:16]([O-:18])=[O:17])[C:12]([O-:14])=[O:13])([OH:8])=[O:7].[Na+].[Na+].[Na+]>Cl>[C:6]([CH2:9][O:10][CH:11]([CH2:15][C:16]([OH:18])=[O:17])[C:12]([OH:14])=[O:13])([OH:8])=[O:7]Participants
3
Reagents, catalysts & solvents 1
Procedure
One hundred grams (0.29 mole) of trisodium carboxymethyloxysuccinate pentahydrate is placed in a flask and acidified with 90 mls of 37% hydrochloric acid while stirring and cooling the mixture in an ice bath. The reaction mixture is then evaporated to dryness in vacuo. The evaporation residue is then taken up in about 150 ml acetone and filtered to remove sodium chloride. The acetone filtrate is next evaporated to dryness to give essentially pure carboxymethyloxysuccinic acid as a residue.
Workup
- temperaturecooling the mixture in an ice bath
- customThe reaction mixture is then evaporated to dryness in vacuo
- filtrationfiltered
- customto remove sodium chloride
- customThe acetone filtrate is next evaporated to dryness
Sources & evidence
- ORD record
- ord-65e8f6b5d1f14f9b831bf436b371f701
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04167523
Reaction notes
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