HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dichlorobenzene-1,2-dicarboxylic acid → 3,5-Dichlorophthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dichlorobenzene-1,2-dicarboxylic acid | HCID 14418781 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,5-Dichlorophthalic anhydride | HCID 104034 | — |
Reaction Steps
3,5-Dichlorophthalic acid (3.36 g, preparation given in Example 1 of U.S. Pat. No. 5,086,188) was refluxed with 10 mL of xylenes while the water generated from the cyclization was collected in a Barrett trap. After refluxing for 5 hours the reaction was cooled, and the xylenes were removed under vacuum. The resultant solids were dried overnight in a vacuum desiccator to give 2.32 g of 3,5-dichlorophthalic anhydride, mp 90° to 94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405995 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-0fc80541e9894187ab85966c7e2e1ab8 |
| Source note | uspto-grants-1995_04 |