HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369558Generated: October 24, 2026
Hydrochloric Acid → 4-Fluoro-4'-(phenylethynyl)benzophenone
https://huagongshe.com/en/reaction/369558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-Bromophenyl)(4-fluorophenyl)methanone | HCID 74951 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Fluoro-4'-(phenylethynyl)benzophenone | HCID 4095657 | — |
Reaction Steps
4-Fluoro-4'-phenylethynylbenzophenone was synthesized by the cuprous iodide catalyzed coupling of 4-bromo-4'-fluorobenzophenone. More specifically, 4-bromo-4'-fluorobenzophenone (30 grams, 0.11 mol), phenylacetylene (11 grams, 0.11 mol), triphenylphosphine (0.2 gram), cuprous iodide (0.1 gram), bis(triphenylphosphine) palladium dichloride (0.1 gram) and 450 milliliters of triethylamine were charged to a 500 milliliter flask equipped with a mechanical stirrer, N2 inlet, and reflux condenser. The mixture was heated to reflux for 4 hours, cooled to 23° C., and stirred for an additional 16 hours. The mixture was then poured into water acidified with HCl and the precipitate was collected by filtration. Recrystallization from acetone gave 23 grams (75 percent yield) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06139920 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-c4709ef325e24f80b7a8bb3c436bd115 |
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| Source note | uspto-grants-2000_10 |
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