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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632065Generated: October 30, 2026

Ethyl Acetate → 3'-Chloro-2-methoxy-1,1'-biphenyl

https://huagongshe.com/reaction/1632065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactanto-IodoanisoleHCID 68257—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3'-Chloro-2-methoxy-1,1'-biphenylHCID 1327063189%

Reaction Steps

A suspension of 2-iodoanisol (3.00 g, 12.8 mmol), 3-chlorophenylboronic acid (2.41 g, 15.4 mmol), and potassium carbonate (3.54 g, 25.6 mmol) in water (10 mL) and methanol (50 mL) was purged with a nitrogen stream for 20 min. To the suspension was added palladium(II) acetate (57.6 mg, 0.2564 mmol) and the solution was stirred at room temperature overnight (18 h). To the reaction was added ethyl acetate (100 mL) and water (100 mL). The layers were separated, the aqueous layer extracted with ethyl acetate (100 mL), and the organic extracts were combined. The organic solution was washed with water (2×150 mL) and brine (150 mL), decolorized with activated charcoal, dried over sodium sulfate, and the solvent removed under reduced pressure. The resulting residue was purified by flash silica gel column chromatography eluting with 10-30% ethyl acetate in hexanes to give I-16 (2.50 g, 89% yield) as colorless oil. 1H NMR (400 MHz CDCl3) 7.53 (t, J=1.8 Hz, 1H), 7.40 (dt, J=7.2 Hz, 1.6 Hz, 1H), 7.38-7.28 (m, 4H), 7.05-6.97 (m, 2H), 3.82 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791267B2
Source datasetuspto-grants-2014_07
ORD IDord-dbdebdc29ce24c05a467198c17eb2a20
Source noteuspto-grants-2014_07