Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Melamine | HCID 7955 | — |
| Product | HCID 21285052 | HCID 21285052 | — |
Reaction Steps
The process for Example 6 was initiated by charging 593.5 g phenol (6.31 moles), 1.2 g of benzoic acid (0.2% of phenol) and 75.2 g melamine (0.60 moles) into a reaction vessel to form a reaction mixture. The reaction mixture was heated to 80° C. and 64.1 g of 50.3% aqueous formaldehyde (60% of total charge) was added over 26 minutes. The reaction mixture was atmospherically distilled to 123° C., maintained at 123° C. for 2 hours, and then reduced to 80° C. 42.5 g of 50.3% aqueous formaldehyde (40% of total charge) was added over about 17 minutes to the reaction mixture, and then atmospherically distilled to 123° C., and then maintaining the temperature at 123° C. for 1.4 hours followed by increasing the temperature over 50 minutes to 165° C. and continuing to distill atmospherically. Next, the reaction mixture was under a gradually increasing vacuum over 2 hours to full vacuum of at least 27 inches while maintaining a temperature of 163°-165° C., followed by heating the reaction mixture to 175° C. under full vacuum. Further, the process is concluded by removing the vacuum distillate (413.7 g) and discharging the product (261.2 g) from the reaction vessel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09249251B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-02b05f771a30490090a94400c444fb50 |
|---|
| Source note | uspto-grants-2016_02 |
|---|