HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bisphenol A → Ether phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | 4-Nitro-N-methylphthalimide | HCID 92321 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Dinatriumphenolat | HCID 15819849 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ether phthalimide | HCID 18959638 | — |
Reaction Steps
Reaction was effected between equal molar amounts of bisphenol-A and sodium methoxide in anhydrous methanol. A mixture of 1.99 part of the resulting sodium bisphenoxide salt, 3.02 part of 4-nitro-N-methylphthalimide, 4.71 parts of tetrabutylammonium bromide which was 2 equivalents, and about 21 parts of toluene, was heated at reflux under nitrogen for 22 hours. The reaction mixture was cooled to room temperature and was extracted with a mixture of methylene chloride and 1.2 normal HCl. The resulting organic solution was dried and concentrated. The resulting mixture was stirred with methanol and filtered resulting in 2.35 parts of an ether phthalimide of the formula, ##STR7## having a melting point of 145°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04273712 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-97c3713e46554e30b4282328653fc470 |
| Source note | uspto-grants-1981_06 |