Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylene Glycol | HCID 1030 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 86751389 | HCID 86751389 | 89% |
Reaction Steps
A three-liter reactor equipped as described in Example 2 is charged with a mixture of maleic anhydride (750 g) and phthalic anhydride (250 g), which is melted by heating to 70° C. Propylene glycol (348 g) is added, and the exothermic reaction is maintained at 130° C. or less until the reaction subsides (about 2 h). The acid number of this bis-maleate/phthalate intermediate is 417 mg KOH/g. A 3000 mol. wt. polyoxypropylene triol (1152 g) and p-toluenesulfonic acid (2.5 g) are added, and the mixture is heated at 190° C. until the acid number drops to 123 mg KOH/g. Propylene glycol (237 g) is added, and heating continues until the acid number reaches 42 mg KOH/g. The product is cooled and isolated (2372 g, 89% yield). GPC analysis shows: Mn =1475, Mw=7590. A blend of the resin with 40 wt. % styrene has APHA color =150.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05677396 |
|---|
| Source dataset | uspto-grants-1997_10 |
|---|
| ORD ID | ord-f96411fccec441f2adb49cd803cf4aa7 |
|---|
| Source note | uspto-grants-1997_10 |
|---|