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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653615Generated: November 2, 2026

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

https://huagongshe.com/reaction/1653615

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 a HCl scrubbing tower, is added 2,5-dichlorobenzoic chloride (4500 g, 21.5 mol) and phenyl ether (5489 g, 32.3 mol). The solution is cooled in ice to 5° C. under stirring, and aluminum chloride (3700 g, 27.8 mol) is added slowly, over a period of about 10 minutes. The temperature of the reaction mixture is about 35° C. after the addition. The mixture is then stirred for about 30 minutes and poured into about 20 gallons of ice water. The large reddish mass is dissolved by adding about 12 L of methylene chloride and stirring. The organic layer is separated and the aqueous layer is extracted with some methylene chloride. After methylene chloride is removed from the combined organic layer by distillation, the residue is 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 is kept for later recovery of remaining product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403675
Source datasetuspto-grants-1995_04
ORD IDord-3ddf9063c201453fac84204e221a006a
Source noteuspto-grants-1995_04