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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600469Generated: October 28, 2026

Hydrochloric Acid → 2,5-Dichloro-4'-phenoxybenzophenone

https://huagongshe.com/reaction/1600469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiphenyl EtherHCID 7583—
Reactant2,5-Dichlorobenzoyl chlorideHCID 17945—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product2,5-Dichloro-4'-phenoxybenzophenoneHCID 1208105973%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a 22 L open-mouth round bottom flask fitted with a three-necked flange head, a mechanical stirrer, a nitrogen inlet and an outlet connected to an HCl scrubbing tower was added 2,5-dichlorobenzoylchloride (4500 g, 21.5 mol) and phenyl ether (5489 g, 32.3 mol). The solution was cooled in ice to 5° C. under stirring and aluminum chloride (3700 g, 27.8 mol) was added slowly. After about 300 g aluminum chloride was added, the solution started to foam violently. The rest was added carefully over about 10 min. On several occasions, the stirring had to be stopped to control the foaming. The temperature of the reaction mixture was about 35° C. after the addition. The mixture was then stirred for about 30 min. and poured into about 20 gallons of ice water. The large reddish mass was dissolved by adding about 12 L of methylene chloride and stirring. The organic layer was separated and the aqueous layer was extracted with some methylene chloride. After methylene chloride was removed from the combined organic layer by distillation, the residue was recrystallized twice from cyclohexane (2×10 L), washed with cooled hexane, air dried and then vacuum dried to afford 5387 g monomer (73%). The mother liquor was kept for later recovery of remaining product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05976437
Source datasetuspto-grants-1999_11
ORD IDord-693a48ed000e4df3a576a90f19c5a1eb
Source noteuspto-grants-1999_11