HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4-Phenoxybenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Terephthaloyl chloride | HCID 7488 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | 4-Phenoxybenzophenone | HCID 238623 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-Phenoxybenzoyl chloride | HCID 74193 | 1,905.3% |
Reaction Steps
p-Phenoxybenzoyl chloride (12.633 g, 0.0543 moles) and BPBPTCDI (3.5459 g, 0.0054 moles) were polymerized with terephthaloyl chloride (1.1572 g, 0.0057 moles) in the presence of aluminum chloride (32.84 g, 0.2463 moles), DMF (10.08 mLs, 0.1308 moles), p-phenoxybenzophenone (0.1646 g, 0.0006 moles) and DCE (120 mLs) initially at -30° C., but warming to room temperature over two hours. The reaction mixture was left at room temperature for fifteen hours and then heated at 28°-32° C. for twenty-six hours. After working up as described in Example 4 the copolymer was obtained as a very pale orange fibrous powder (14.33 g, 95.2% yield), IV 0.90 dl/g (c=0.12 g/dL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868271 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-1256bd5d2b314e7c8a744744f425e383 |
| Source note | uspto-grants-1989_09 |