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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902298Generated: October 27, 2026

Potassium Carbonate → 2',6'-Dichloro-2-methoxybiphenyl

https://huagongshe.com/reaction/902298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-2,6-dichlorobenzeneHCID 29568—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
CatalystBis(tri-o-tolylphosphine)palladium(II) DichlorideHCID 10876480—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2',6'-Dichloro-2-methoxybiphenylHCID 5415141749.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-bromo-2,6-dichlorobenzene (5.0 g, 0.022 mol), 2-methoxyphenylboronic acid (5.045 g, 0.033 mol) and potassium carbonate (7.65 g, 0.055 mol) in dioxane (130 mL) and water (13 mL) was purged with nitrogen for 20 minutes. Trans-dichlorobis(tri-o-tolylphosphine)palladium (II) (0.87 g, 0.0011 mol) was added and the reaction mixture heated to 100° C. for 36 hours. The cooled reaction mixture was then filtered through celite washing the filter cake with ethyl acetate. The combined organic filtrates were diluted to 500 mL by the addition of ethyl acetate, then washed with 2.0 M aqueous sodium hydroxide (2×350 mL), water (350 mL) and saturated brine (350 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a yellow oil. Purification by flash chromatography using a solvent gradient of 0.5 to 2% ethyl acetate in hexane gave 2.74 g (49%) of 2′,6′-dichloro-1,1′-biphenyl-2-yl methyl ether as a white solid. MS (EI) m/z 252 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365095B2
Source datasetuspto-grants-2008_04
ORD IDord-33c104223afd44648e4e55f7dffb268c
Source noteuspto-grants-2008_04