Ethylene Glycol → HCID 131710010, compound

HRID 1729647Notes

Reaction equation

HRID 1729647 reaction equation
[S:1]([C:5]1[C:6]([O:8]C(=O)C=1)=[O:7])([OH:4])(=[O:3])=[O:2].[CH2:12]([OH:15])[CH2:13][OH:14].[OH-:16].[Na+:17].[CH3:18][C:19](C)=[O:20]>O>[OH:20][CH:19]([O:14][CH:13]([CH:5]([S:1]([OH:4])(=[O:2])=[O:3])[C:6]([O-:8])=[O:7])[C:12]([O-:16])=[O:15])[CH3:18].[Na+:17].[Na+:17].[Na+:17]

Participants

6

Reactant 4

HCID 174Ethylene GlycolHCID 180AcetoneHCID 14798Sodium HydroxideHCID 124798802,5-Dioxo-2,5-dihydrofuran-3-sulfonic acid

Product 1

HCID 131710010HCID 131710010, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
80 °C

Procedure

Sulfomaleic anhydride (20 gm) is mixed with 37.2 gm (0.6 mole) of ethylene glycol and heated at 80° C for 4 hours. A solution of 16 gm (0.4 mole) of sodium hydroxide in 75 ml of water is then added and the mixture heated at 80° C for 4 hours. The mixture is then mixed with acetone to precipitate trisodium α-hydroxyethoxy-β-sulfosuccinate, which is purified by repeated extractions with hot acetone to remove all ethylene glycol and water followed by filtration and drying in an oven.

Workup

  1. temperaturethe mixture heated at 80° C for 4 hours
  2. customto precipitate trisodium α-hydroxyethoxy-β-sulfosuccinate, which
  3. customis purified
  4. extractionextractions with hot acetone
  5. customto remove all ethylene glycol and water
  6. filtrationfollowed by filtration
  7. customdrying in an oven

Sources & evidence

ORD record
ord-3efff7777e434bb8bef30629a75080e7
Source dataset
uspto-grants-1976_11
Patent number
US03989700

Reaction notes

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