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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Trimesoyl chloride | HCID 78138 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | [3,5-Bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone | HCID 3302339 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807759B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-042bf47390bb40fd83c61f958c290906 |
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| Source note | uspto-grants-2010_10 |
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