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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428796Generated: October 25, 2026

4-Chloro-o-xylene → 2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenone

https://huagongshe.com/reaction/428796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-o-xyleneHCID 32886—
ReactantOxalyl chlorideHCID 65578—
Reactant4,4'-Carbonyldiphthalic anhydrideHCID 75498—
Product2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenoneHCID 15027172—

Reaction Steps

The benzophenonetetracarboxylic dianhydrides are readily available from commercial sources or synthesis. For instance, 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) 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 is available from 4-chloro-o-xylene by Friedel-Crafts acylation with oxalyl chloride to give 2,2′-dichloro-4,4′,5,5′,-tetramethylbenzophenone, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313348B1
Source datasetuspto-grants-2001_11
ORD IDord-36836eaca2ee4bf8a7d639e2ae81e83f
Source noteuspto-grants-2001_11