HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885657Generated: October 30, 2026
Hydrochloric Acid → [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone
https://huagongshe.com/reaction/1885657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Terephthaloyl chloride | HCID 7488 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone | HCID 11141804 | 88% |
Reaction Steps
Anhydrous aluminum chloride (80.0 g, 0.60 mol) was added to a stirred solution of terephthaloyl chloride (50.8 g, 0.25 mol) dissolved in fluorobenzene (235 ml, 2.5 mol) over a 10-15 minute period. The mixture was stirred at room temperature for one hour and then maintained at 70°-80° C. for four hours. After cooling, the reaction mixture was poured onto approximately 1000 g of ice containing 100 ml of concentrated hydrochloric acid. The resulting suspension was separated by decantation and washed several times with water. The organic layer was distilled to remove excess fluorobenzene and the solid residue collected by filtration, washed with water, and dried at 100° C. The crude solid was recrystallized from approximately 2000 ml of toluene to afford 70.7 g (88% yield) of 1,4-bis(4-fluorobenzoyl)-benzene; mp 218.5°-219.5° C.; Anal. Calcd for C20H12F2O2 : C, 74.53%; H, 3.75%; F, 11.179%. Found: C, 74.60%; H, 3.80%; F, 11.83%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05145937 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-0896f7a069114cef8c71882a43293ed7 |
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| Source note | uspto-grants-1992_09 |
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