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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983725Generated: October 26, 2026

Hydrochloric Acid → 2,5-Bis(4-hexylbenzoyl)terephthalic acid

https://huagongshe.com/reaction/983725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyromellitic dianhydrideHCID 6966—
ReactantHexylbenzeneHCID 14109—
ReactantDiisopropylethylamineHCID 81531—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2,5-Bis(4-hexylbenzoyl)terephthalic acidHCID 22269453—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a mixture of 25.7 grams of aluminum chloride, 51.3 mL of 1,2-dichloroethane, and 10 grams of benzene-1,2,4,5-tetracarboxylic acid dianhydride (pyromellitic dianhydride) was added with cooling, a solution of 14.9 grams of hexylbenzene and 6.40 grams of diisopropylethylamine in 25 mL of 1,2-dichloroethane over a period of 3.5 hours, keeping the temperature between 15° C. and 20° C. The resulting mixture was stirred for an additional 15 minutes after the addition was complete, and it was then heated to 40° C. for one hour. The warm mixture was poured into a beaker with 200 grams of ice and 75 mL of concentrated hydrochloric acid and stirred overnight at room temperature. The aqueous phase was poured off and the resulting oily solid was stirred with 500 mL of water, and the water was poured off. This water wash was repeated, and the resulting residue was dissolved in 250 mL of acetone and concentrated in vacuo. This residue was stirred with 55 mL of ethyl acetate, and the resulting solid was collected by filtration, washed with 100 mL of ethyl acetate, and dried to give 2,5-bis(4-hexylbenzoyl)terephthalic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864396B2
Source datasetuspto-grants-2005_03
ORD IDord-f5f81bd6fa234b2d8d8e6716c744838b
Source noteuspto-grants-2005_03