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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860272Generated: November 2, 2026

4-Chlorophthalic anhydride → HCID 54187688, compound

https://huagongshe.com/reaction/1860272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophthalic anhydrideHCID 67044—
ReactantHCID 18627202HCID 18627202—
ProductHCID 54187688HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528663B1
Source datasetuspto-grants-2003_03
ORD IDord-cce0fa46299d4f1092d0d3503a195399
Source noteuspto-grants-2003_03