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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654276Generated: November 2, 2026

3,5-Dichlorobenzene-1,2-dicarboxylic acid → 3,5-Dichlorophthalic anhydride

https://huagongshe.com/reaction/1654276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzene-1,2-dicarboxylic acidHCID 14418781—
SolventWaterHCID 962—
Product3,5-Dichlorophthalic anhydrideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405995
Source datasetuspto-grants-1995_04
ORD IDord-0fc80541e9894187ab85966c7e2e1ab8
Source noteuspto-grants-1995_04