HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophthalic anhydride → HCID 54187688, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophthalic anhydride | HCID 67044 | — |
| Reactant | HCID 18627202 | HCID 18627202 | — |
| Product | HCID 54187688 | HCID 54187688 | — |
Reaction Steps
4-Chlorophthalic anhydride is an expensive starting material which presently must be custom synthesized. Current routes for the synthesis of 4-chlorophthalic anhydride lead to mixtures of isomers, which are difficult to separate, or are prohibitively costly. For example, the Diels-Alder condensation of maleic anhydride with 2-chloro-1,3-butadiene to yield 4-chlorotetrahydrophthalic anhydride, followed by aromatization in the presence bromine requires the subsequent recovery of HBr. Attempted thermal aromatization of 4-chloro-tetrahydrophthalic anhydride results in low yields of 4-chlorophthalic anhydride and tar formation. This and other routes are described in U.S. Pat. Nos. 5,059,697; 5,003,088; 5,322,954; 4,978,760 and 5,233,054.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528663B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-cce0fa46299d4f1092d0d3503a195399 |
| Source note | uspto-grants-2003_03 |