Barium(2+) dichloride → HCID 88051539, compound

HRID 2307194Notes

Reaction equation

HRID 2307194 reaction equation
[Na+].[S:2]([C:6]1[CH:7]=[C:8]([C:15]([O-:17])=[O:16])[CH:9]=[C:10]([CH:14]=1)[C:11]([O-:13])=[O:12])([OH:5])(=[O:4])=[O:3].[Na+].[Na].[Cl-].[Ba+2:21].[Cl-]>O>[Ba+2:21].[S:2]([C:6]1[CH:7]=[C:8]([C:15]([O-:17])=[O:16])[CH:9]=[C:10]([CH:14]=1)[C:11]([O-:13])=[O:12])([OH:5])(=[O:4])=[O:3]

Participants

5

Reactant 3

HCID 5360350Barium(2+) dichlorideHCID 5360545SodiumHCID 21881961HCID 21881961, compound

Product 1

HCID 88051539HCID 88051539, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent3×

Conditions

Temperature
30 °C

Procedure

268 Grams of 5-sulfoisophthalic acid sodium salt were placed together with 1600 g of ion exchanged water in a reactor equipped with a stirrer. The contents in the reactor were heated with stirring to 80° C. so that the sodium salt was dissolved in water. A solution of barium chloride dissolved in an amount of 104 g into 900 ml of ion exchanged water was then gradually added dropwise to the thus obtained solution. The resulting mixture was cooled to 30° C. and filtered to separate white precipitates. The precipitates were dispersed in 3000 g of ion exchanged water. The dispersion was heated to 80° C., maintained at that temperature for 1 hour, cooled to 30° C. and then filtered. The precipitates were washed with water. Such a procedure including dispersion, heating, filtration and washing steps was repeated once more. The thus obtained precipitates were dried at 120° C. for 5 hours to obtain 265 g of 5-sulfoisophthalic acid barium salt as a white powder. The atomic absorption analysis revealed that the 5-sulfoisophthalic acid barium salt powder contained 21.9% by weight of barium and 120 ppm by weight of sodium.

Workup

  1. customequipped with a stirrer
  2. temperatureThe contents in the reactor were heated
  3. additionwas then gradually added dropwise to the thus obtained solution
  4. filtrationfiltered
  5. customto separate white precipitates
  6. additionThe precipitates were dispersed in 3000 g of ion
  7. temperatureThe dispersion was heated to 80° C.
  8. temperaturemaintained at that temperature for 1 hour
  9. temperaturecooled to 30° C.
  10. filtrationfiltered
  11. washThe precipitates were washed with water
  12. temperatureheating
  13. filtrationfiltration
  14. washwashing steps
  15. customThe thus obtained
  16. customprecipitates
  17. customwere dried at 120° C. for 5 hours

Sources & evidence

ORD record
ord-6f0b8f7024a6471f8480878793a5de10
Source dataset
uspto-grants-2004_12
Patent number
US06830859B2

Reaction notes

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