Melamine → HCID 131724601, compound
Reaction equation
[N:1]1[C:8]([NH2:9])=[N:7][C:5]([NH2:6])=[N:4][C:2]=1[NH2:3].[C:10]1([P:16]([Cl:24])([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>CN(C)C(=O)C>[C:10]1([P:16]([Cl:24])([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:17])[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1.[N:1]1[C:8]([NH2:9])=[N:7][C:5]([NH2:6])=[N:4][C:2]=1[NH2:3]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 120 °C
Procedure
To an one liter four-inlet flask equipped with a thermocouple and temperature controller, a reflux condenser, a nitrogen feed and a mechanical stirrer, 1 mole (126 g) Melamine (MA) and 500 ml N,N-dimethylacetamide (DAMc) were added, heated to 120° C. and then stirred until MA was dissolved completely. 1 mole (253 g) diphenyl phosphoryl chloride (DPC) was added slowly to the resulting solution. The mixture was heated gradually to a temperature of 168° C. when the addition of DPC was completed. The reaction was continued for 10 hours. The reaction mixture was cooled and filtered, and the resulting cake was dried to obtain DPC-MA (P-14). Molecular weight: 558. Yield, 94%; softening temperature, 131-135° C. Phosphorus content: 9.05%. Nitrogen content: 24.53%.
Workup
- customTo an one liter four-inlet flask equipped with a thermocouple and temperature controller, a reflux condenser
- dissolutionwas dissolved completely
- temperatureThe mixture was heated gradually to a temperature of 168° C. when
- temperatureThe reaction mixture was cooled
- filtrationfiltered
- customthe resulting cake was dried
Sources & evidence
- ORD record
- ord-5639d1a9ea304ad18e01a52e7640bb1d
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06797821B2
Reaction notes
Loading…