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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113015Generated: October 29, 2026

Potassium Carbonate → HCID 11654119, compound

https://huagongshe.com/reaction/2113015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Phenoxyphenyl)boronic acidHCID 2773559—
ReactantMethyl 3-((4-iodophenoxy)methyl)benzoateHCID 57643351—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11654119HCID 11654119—

Reaction Steps

A degassed solution of 3-(4-iodo-phenoxymethyl)-benzoic acid methyl ester (of Inter-mediate 1; 74 mg, 0.2 mmol) in dioxane (4 mL) and a degassed solution of potassium carbonate (83 mg) in water (0.4 mL) were added to a reaction vial containing (2-phenoxy)phenylboronic acid (available from Aldrich Chemical Company, Inc., Milwaukee, Wis.; 128 mg, 0.6 mmol). The solution was degassed and bis(tri-cyclohexylphos-phine)palladium (available from Strem Chemicals, Inc., Newburyport, Mass.; 7 mg, 0.01 mmol) was added. The mixture was heated in a microwave oven at 170 degrees for 25 min. The reaction mixture was filtered through silica, and washed with dioxane (1 mL) and dimethylacetamide (1 mL). 2 M potassium hydroxide solution (0.4 mL) was added. The mixture was stirred at room temperature overnight, and then 1 M HCl (0.8 mL) was added. The solvent was evaporated and the residue was triurated with 50% aqueous methanol to give 3-(2′-phenoxy-biphenyl-4-yloxymethyl)-benzoic acid. Mass spectrum MH+=397.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524870B2
Source datasetuspto-grants-2009_04
ORD IDord-a8d3e094973946e8921407033350a48b
Source noteuspto-grants-2009_04