HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxyphenol → HCID 19876214, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | 4-Nitrobenzil | HCID 283893 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 19876214 | HCID 19876214 | — |
Reaction Steps
Equimolar amounts of 4-nitrobenzil and 4-phenoxyphenol are reacted in the presence of potassium t-butoxide under conditions described in Example 56 paragraph (d) to form 4-(phenoxyphenoxy)benzil. A polyquinoxaline terminated by aromatic groups which are susceptible to aromatic electrophilic substitution is synthesized by the reaction of p-BOB from Example 56, -(phenoxyphenoxy)benzil and 3,3',4,4'-tetraaminobiphenyl in m-cresol. The resulting polyquinoxaline polymer is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05098985 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-7a315c1a3b154764bf361f31b824644b |
| Source note | uspto-grants-1992_03 |