Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158210Generated: October 25, 2026

Dichloromethane → [3,5-Bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone

https://huagongshe.com/reaction/1158210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantFluorobenzeneHCID 10008—
ReactantTrimesoyl chlorideHCID 78138—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product[3,5-Bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanoneHCID 330233970%

Reaction Conditions

Temperature25 °C

Reaction Steps

5 g of 1,3,5-benzenetricarbonyltrichloride (18.8 mol), 6.7 g of aluminum chloride (50.0 mmol) and 50 mL of distilled dichloromethane (DCM) were put in a 250 mL round flask, which was stirred for 30 minutes at 25° C. for reaction in the presence of nitrogen. 20 mL of dichloromethane and 4.5 g of fluorobenzene (48.8 mmol) were added in 100 mL of Dropping funnel, and the fluorobenzene solution was dropped in the round flask drop by drop. The reaction mixture was stirred for 4 hours in the presence of nitrogen, to which 20 mL of distilled water was added. The reaction mixture was stirred further for more than 12 hours. The organic layer of the reaction mixture was extracted by using dichloromethane, and the organic solvent was eliminated, resulting in a crude product. The crude product was re-crystallized using ethanol to give white brancher [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl) methanone (yield: 70%). The structure of the [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone was confirmed by 1H-NMR, 13C-NMR spectrometry and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807759B2
Source datasetuspto-grants-2010_10
ORD IDord-042bf47390bb40fd83c61f958c290906
Source noteuspto-grants-2010_10