HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250526Generated: November 2, 2026
Water → 4-(Trifluoromethoxy)-4'-methoxy-1,1'-biphenyl
https://huagongshe.com/reaction/250526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-(trifluoromethoxy)benzene | HCID 521008 | — |
| Reactant | 2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 584319 | — |
| Catalyst | HCID 178477754 | HCID 178477754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Trifluoromethoxy)-4'-methoxy-1,1'-biphenyl | HCID 11173203 | 193.9% |
Reaction Steps
To a solution of 1-bromo-4-(trifluoromethoxy)benzene (0.90 g, 3.7 mmol) in tetrahydrofuran (20 ml) was added a solution of 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.36 g, 1.54 mmol) in tetrahydrofuran (10 ml), potassium carbonate (0.42 g, 3.0 mmol), [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (40 mg, 0.077 mmol) and water (0.20 ml) and the mixture refluxed under nitrogen for 19 h. The reaction mixture was tipped into water (150 ml) and extracted with ether (2×50 ml), the ether extract then dried (MgSO4) and evaporated to give a tan semi-solid (0.801 g). Purification by column chromatography (silica gel, 4:1 hexane/chloroform) afforded 4-methoxy-4′-(trifluoromethoxy)-1,1′-biphenyl (36) as a white solid (0.33 g, 80%). 1H nmr (CDCl3, 300 MHz) 3.86, s, 4-OMe; 6.99, d (8.7 Hz), H3,5; 7.26, d (8.1 Hz), H3′,5′; 7.49, d (8.7 Hz), H2,6 or H2′,6′; 7.55, d (8.7 Hz), H2′,6′ or H2,6. APCI (+ve) MS m/z 268 (M+, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863313B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-264939122f4147899685375cb376787d |
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| Source note | uspto-grants-2011_01 |
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