Formaldehyde → Melamine formaldehyde
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
Reactant 2
Product 1
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
- customis reacted at pH about 8 to 9
- customa temperature of about 50 to 90° C.
- customwith progress of condensation reaction
- customthe condensation reaction
- temperaturecooling at a suitable stage
- customThis reaction mixture is dried by a spray-drying or other method
- customto provide a particulate crude melamine-formaldehyde condensate
- 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
- custompreferably about 30 min. to 1 hr
- filtration) and filtered
- dissolutionThe residue is dissolved in dimethyl sulfoxide
- filtrationThis dimethyl sulfoxide solution is filtered
- customto remove the insoluble matter
- additionthe filtrate is poured in a large excess of acetone
- filtrationThe precipitate is recovered by filtration
- customdried
Sources & evidence
- ORD record
- ord-c92f857b603441789155c45fdbe46542
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07041718B2
Reaction notes
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