HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-o-xylene → 2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-o-xylene | HCID 32886 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4,4'-Carbonyldiphthalic anhydride | HCID 75498 | — |
| Product | 2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenone | HCID 15027172 | — |
Reaction Steps
Specific benzophenonetetracarboxylic dianhydrides preferred in this invention are readily available from commercial sources or synthesis. For instance, 3,3',4,4'-benzophenonetetracarboxylic dianhydride (D1) is available from Aldrich Chemical Co., Inc. (1001 W. St. Paul Ave., Milwaukee, Wis. 53233). 2,2'-Dichloro-4,4',5,5'-benzophenone tetracarboxylic dianhydride (D2) is available from 4-chloro-o-xylene by Friedel-Crafts acylation with oxalyl chloride to give 2,2'dichloro-4,4',5,5',-tetramehtylbenzophenone, followed by oxidation with nitric acid and dehydration of the resulting tetracarboxylic acid as described by Falcigno, et al., J. Poly. Sci. 1992, 30, 1433.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817743 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-29940d58e9204e7f9f7e7142cf74b95f |
| Source note | uspto-grants-1998_10 |