HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101232Generated: October 25, 2026
1-(4'-Fluoro(1,1'-biphenyl)-4-yl)ethanone → 4-(4-Fluorophenyl)benzoic acid
https://huagongshe.com/reaction/2101232
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4'-Fluoro(1,1'-biphenyl)-4-yl)ethanone | HCID 608114 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Acetic acid;1,1'-biphenyl | HCID 21957439 | — |
| Reactant | sodium hypobromite | HCID 178507097 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4-Fluorophenyl)benzoic acid | HCID 2782689 | — |
Reaction Steps
NaOH (7 g) was dissolved in water (25 mL) and cooled in an ice bath. Bromine (7.8 g) was added dropwise to give a solution of NaOBr. 1-(4′-Fluoro-biphenyl-4-yl)-ethanone (0.01 mol) was dissolved in dioxane (35 mL) and warmed to 50° C. in a water bath. The NaOBr solution was added slowly to the stirred solution of the biphenyl acetate and stirring continued at 50° C. for a further 20 minutes. The solution was allowed to cool and a solution of sodium metabisulphite (8 g in 40 mL water) was added followed by water (170 mL). 50 mL of the liquid was evaporated under reduced pressure with heating. The remainder was acidified with HCl (5 mL) and a white precipitate formed upon cooling. The precipitate was filtered and recrystallised from acetic acid to give the title compound. δC (CDCl3, 62.9 MHz): 115.9, 126.8, 129.2, 129.6, 129.8 (d, J 2.9), 135.5 (d, J 2.9), 143.2, 162.4 (d, J 245.1) and 167.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572825B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-f4e8cebf7e8249d6b95b7196fbd0c0bd |
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| Source note | uspto-grants-2009_08 |
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