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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
Reactant2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 584319—
CatalystHCID 178477754HCID 178477754—
SolventTetrahydrofuranHCID 8028—
Product4-(Trifluoromethoxy)-4'-methoxy-1,1'-biphenylHCID 11173203193.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863313B2
Source datasetuspto-grants-2011_01
ORD IDord-264939122f4147899685375cb376787d
Source noteuspto-grants-2011_01