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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336240Generated: October 29, 2026

Potassium Carbonate → Methyl 2'-methoxy-2-methylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/336240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
ReactantMethyl 4-bromo-3-methylbenzoateHCID 3294148—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl 2'-methoxy-2-methylbiphenyl-4-carboxylateHCID 6752878080%

Reaction Steps

A suspension of methyl 4-bromo-3-methylbenzoate (4.9 g; 21.4 mmol; 1 eq.), 2-methoxyphenylboronic acid (Aldrich 44, 523-1; 3.6 g; 23.5 mmol; 1.1 eq.), potassium carbonate (14.8 g; 107 mmol; 5 eq.) and Pd(PPh3)4 (2.47 g; 2.14 mmol; 0.1 eq.) in toluene (24.5 mL) and water (24.5 mL) was refluxed for 6 hours. The reaction mixture was cooled down to room temperature and filtered through a pad of CELITE which was further washed with toluene (500 mL). The filtrate was concentrated in vacuo and the residue taken up in ethyl acetate (500 mL). The organic layer was washed with sat. aq. NaHCO3 (200 mL), water (200 mL) and brine (200 mL) then dried over magnesium sulfate and concentrated in vacuo. The crude was purified by column chromatography (c-hexane/ethyl acetate, 90/10) to afford the title compound (4.38 g, 80%) as a colorless oil. HPLC (Method A): Rt 4.85 min (purity 98.9%). LC/MS: 257.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889668B2
Source datasetuspto-grants-2014_11
ORD IDord-2b85fdc295054511b9a04848deb94616
Source noteuspto-grants-2014_11