Formaldehyde → Melamine formaldehyde

HRID 1824292Notes

Reaction equation

HRID 1824292 reaction equation
[CH2:1]=[O:2].[N:3]1[C:10]([NH2:11])=[N:9][C:7]([NH2:8])=[N:6][C:4]=1[NH2:5]>>[CH2:1]=[O:2].[N:3]1[C:10]([NH2:11])=[N:9][C:7]([NH2:8])=[N:6][C:4]=1[NH2:5]

Participants

3

Procedure

The melamine resin (1) is disclosed in Japanese Patent Application Laid-open No. 73267/1994 (JP-A-6-73267) and can be produced by reacting about 0.8 to 10 moles (preferably 0.8 to 5 moles, more preferably 1 to 3 moles, and particularly 1 to 2 moles) of formaldehyde with each mole of melamine in aqueous solution or aqueous dispersion. Thus, for example, a mixture of melamine with an aqueous solution of formaldehyde is reacted at pH about 8 to 9 and a temperature of about 50 to 90° C. and as the solution develops turbidity with progress of condensation reaction, the condensation reaction is stopped by, for example, cooling at a suitable stage. This reaction mixture is dried by a spray-drying or other method to provide a particulate crude melamine-formaldehyde condensate. This particulate crude melamine-formaldehyde condensate is washed with warm water (about 50 to 70° C.) for a suitable time (e.g. 10 min. to 3 hrs., preferably about 30 min. to 1 hr.) and filtered. The residue is dissolved in dimethyl sulfoxide. This dimethyl sulfoxide solution is filtered to remove the insoluble matter and the filtrate is poured in a large excess of acetone. The precipitate is recovered by filtration and dried to provide a purified melamine-formaldehyde polycondensate as white powders.

Workup

  1. customis reacted at pH about 8 to 9
  2. customa temperature of about 50 to 90° C.
  3. customwith progress of condensation reaction
  4. customthe condensation reaction
  5. temperaturecooling at a suitable stage
  6. customThis reaction mixture is dried by a spray-drying or other method
  7. customto provide a particulate crude melamine-formaldehyde condensate
  8. washThis particulate crude melamine-formaldehyde condensate is washed with warm water (about 50 to 70° C.) for a suitable time (e.g. 10 min. to 3 hrs
  9. custompreferably about 30 min. to 1 hr
  10. filtration) and filtered
  11. dissolutionThe residue is dissolved in dimethyl sulfoxide
  12. filtrationThis dimethyl sulfoxide solution is filtered
  13. customto remove the insoluble matter
  14. additionthe filtrate is poured in a large excess of acetone
  15. filtrationThe precipitate is recovered by filtration
  16. customdried

Sources & evidence

ORD record
ord-c92f857b603441789155c45fdbe46542
Source dataset
uspto-grants-2006_05
Patent number
US07041718B2

Reaction notes

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