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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269565Generated: October 25, 2026

Potassium Carbonate → Ethyl 5-chloro-2''-[(phenylmethyl)oxy]-1,1':2',1''-terphenyl-2-carboxylate

https://huagongshe.com/reaction/269565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantToluene ethanolHCID 21863594—
ReactantEthyl 2-bromo-4-chlorobenzoateHCID 53216606—
Reactant2'-Benzyloxy-biphenyl-2-boronic acidHCID 58730990—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthyl 5-chloro-2''-[(phenylmethyl)oxy]-1,1':2',1''-terphenyl-2-carboxylateHCID 58731013—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2′-benzyloxybiphenyl boronic acid (50 mg, 0.16 mmol), ethyl 2-bromo-4-chlorobenzoate (66 mg, 0.25 mmol), potassium carbonate (88 mg, 0.64 mmol) and tetrakis(triphenylphosphine)palladium(0) (10 mg, 5 mol %) in 1:1 toluene/ethanol (2 ml) was stirred and heated at 90° C. under nitrogen for 12 hours. After cooling the mixture was diluted with diethyl ether and water and the organic phase dried (MgSO4) and evaporated to dryness. The residue was chromatographed with ethyl acetate/iso-hexane (1:9) to yield the title compound as a pale yellow gum. (46 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446222B2
Source datasetuspto-grants-2008_11
ORD IDord-a36b5c992b014a60a613a74fb93c144b
Source noteuspto-grants-2008_11