HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619697Generated: November 1, 2026
Water → 2-Chloro-2'-fluoro-5-methoxybiphenyl
https://huagongshe.com/reaction/1619697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | 2-Bromo-1-chloro-4-methoxybenzene | HCID 24212081 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-2'-fluoro-5-methoxybiphenyl | HCID 58042298 | 88.6% |
Reaction Steps
Tetrakistriphenylphosphinepalladium (0) (229 mg, 0.20 mmol) was added to a degassed mixture of 2-fluorophenylboronic acid (556 mg, 3.97 mmol), 2-bromo-1-chloro-4-methoxybenzene (0.49 mL, 3.57 mmol), caesium carbonate (3.87 g, 11.9 mmol), water (5.0 mL) and dioxane (26.0 mL). The reaction was heated at 80° C. for 18 hours, cooled to room temperature and then partitioned between ethyl acetate (30.0 mL) and sat. aq. ammonium chloride (10.0 mL). The aqueous phase was separated and extracted with ethyl acetate (2×10 mL). The combined organic phases were washed with brine (5.0 mL), dried over MgSO4, filtered and evaporated to give a pale yellow oil. Column chromatography purification on silica, eluting with heptanes gave the title compound (749 mg, 88%) as a colourless oil.
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-d8d4b2361e5147d793efdc9c007bc1eb |
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| Source note | uspto-grants-2014_07 |
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