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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902298Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/902298

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-Bromo-2,6-dichlorobenzeneHCID 29568—
Edukt2-Methoxyphenylboronic acidHCID 2733958—
KatalysatorBis(tri-o-tolylphosphine)palladium(II) DichlorideHCID 10876480—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2',6'-Dichloro-2-methoxybiphenylHCID 5415141749,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07365095B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-33c104223afd44648e4e55f7dffb268c
Quellennotizuspto-grants-2008_04