Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388239Generated: October 30, 2026

Benzene → 1,4-Dibenzoylbenzene

https://huagongshe.com/reaction/1388239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
ReactantTerephthaloyl chlorideHCID 7488—
ReactantAluminum(III) ChlorideHCID 6451240—
Product1,4-DibenzoylbenzeneHCID 76395—

Reaction Steps

To a stirred slurry of 56 g of aluminum chloride in 150 ml of benzene under reflux was added dropwise 40 g of terephthaloyl chloride dissolved in 250 ml of benzene. When the addition was complete the reaction was refluxed for 15 minutes, cooled, and 250 ml of water was added slowly. The benzene layer was separated and the aqueous layer was extracted with methylene chloride (2×300 ml). The combined organic layers were washed with 1 M NaOH solution (2×400 ml) and water (400 ml), dried (MgSO4), filtered, and the solvents were removed under reduced pressure to a nearly colorless solid. Recrystallization from 95% ethanol gave 46.8 g of colorless 1,4-dibenzoylbenzene, m.p. 160°-162°. Reduction of 20 g of this material with 1.8 g of sodium borohydride in 250 ml of ethanol gave 14.2 g of colorless 1,4-dibenzylolbenzene m.p. 142°-145°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431497
Source datasetuspto-grants-1984_02
ORD IDord-708d032b71aa402fabefe0ec17e34042
Source noteuspto-grants-1984_02