HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044765Generated: October 30, 2026
Sodium Carbonate → 2,3',4',5'-Tetrafluorobiphenyl-4-ol
https://huagongshe.com/reaction/2044765
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-3-fluorophenol | HCID 2779153 | — |
| Reactant | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Reactant | HCID 21870694 | HCID 21870694 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,3',4',5'-Tetrafluorobiphenyl-4-ol | HCID 21052144 | 81.5% |
Reaction Steps
At first, 75.0 g of 4-bromo-3-fluorophenol (S3-1), 82.9 g of 3,4,5-trifluorophenyl-boric acid (S3-2), 13.6 g of tetrakis(triphenylphosphine)palladium, 108.5 g of sodium carbonate and 1100 ml of a mixed solvent of dimethoxyethane/water=2/1 (volume ratio) were added into a reactor under nitrogen atmosphere, and the mixture was heated to 80° C. and stirred for 4 hr. Next, the reaction solution was cooled to room temperature, added with toluene and then washed with 1N hydrochloric acid and water. Afterwards, the solution was dried over magnesium sulfate and distilled under reduced pressure to remove the solvent. Subsequently, the product was purified by silica-gel column chromatography with a mixed solvent of heptane/ethyl acetate=4/1 as the eluent and then dried under reduced pressure. The obtained residue was recrystallized in heptane to obtain 77.5 g of 3-fluoro-4-(3,4,5-trifluorophenyl)phenol (S3-3). The yield of (S3-3) from (S3-1) was 81.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586803B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f756be29c2214a45949dfd1698a182ee |
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| Source note | uspto-grants-2013_11 |
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