HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619664Generated: October 30, 2026
Water → 4′-Chloro-3′-(trifluoromethyl)[1,1′-biphenyl]-4-ol
https://huagongshe.com/reaction/1619664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzeneboronic acid | HCID 2782671 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4′-Chloro-3′-(trifluoromethyl)[1,1′-biphenyl]-4-ol | HCID 23005088 | 27.5% |
Reaction Steps
4-Chloro-3-(trifluoromethyl)phenylboronic acid (448 mg, 2 mmol) and 4-iodophenol (440 mg, 2 mmol) were dissolved in dioxane (10 mL). Caesium carbonate (1.95 g, 6 mmol), water (2 mL) and tetrakis(triphenylphosphine)palladium (0) (231 mg, 0.2 mmol) were added and the reaction stirred at 80° C. for 1 hour. The reaction was quenched with 2M HCl (5 mL) and partitioned between ethyl acetate (50 mL) and water (50 mL). The ethyl acetate was separated, dried over MgSO4 and evaporated. The crude product was chromatographed on silica eluting with a gradient of heptane:ethyl acetate 100:0 to 80:20 to give the title compound (150 mg, 0.55 mmol, 27%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772293B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-3307399c6f5a4f26bf5a0fc075e89d7a |
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| Source note | uspto-grants-2014_07 |
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