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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248655Generated: October 30, 2026

1,4-Dichlorobenzene → 2,5-Dichlorobenzophenone

https://huagongshe.com/reaction/248655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DichlorobenzeneHCID 4685—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product2,5-DichlorobenzophenoneHCID 45818880%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 22 L, three-necked flask fitted with a thermometer, mechanical stirrer and a Vigreux column connected to an aqueous NaOH scrubbing tower, was added 1,4-dichlorobenzene (3 Kg, 26.4 mol) and benzoyl chloride (2.6 Kg, 18.55 mol). The mixture was heated to 80° C. to give a homogeneous solution. Aluminum chloride (5.5 Kg, 41.25 mol) was added over 12 min. with stirring. (The molar ratio of reactants was 2.2:1.4:1.0 (AlCl3 : Dichlorobenzene:Benzoyl Chloride)). The resulting mixture was heated to 140° C. over 60 min followed by heating to 175° C. over 30 min. Heating was stopped at 175° C. The mixture was allowed to cool to 80° C. over two hours and poured into a well stirred mixture of ice and water (ca. 25 L water and 15 Kg of ice) over 30 min. The organic solid was collected by filtration and dissolved in 7 L of toluene. The solution was washed with aqueous sodium bicarbonate and dried. Toluene was removed by distillation. Pure 2,5-dichlorobenzophenone was isolated in 80% yield after recrystallization from hexane and toluene. Gas chromatography indicated an absolute yield of 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210313
Source datasetuspto-grants-1993_05
ORD IDord-4585f56064884c37a14842326880a65e
Source noteuspto-grants-1993_05