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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444260Generated: November 1, 2026

Phenylboronic Acid → 5-Phenylfuran-2-carboxylic acid

https://huagongshe.com/reaction/1444260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 5-bromofuran-2-carboxylateHCID 599633—
Product5-Phenylfuran-2-carboxylic acidHCID 736255—

Reaction Steps

5-Bromo-furan-2-carboxylic acid methyl ester (5) (205 mg, 1 mmol) was coupled to phenylboronic acid (146 mg, 1.2 mmol) using Method E except that once the reaction was complete, the solvents were removed in vacuo. The crude residue was re-dissolved in EtOAc (10 ml) and 1M NaOH (20 ml) was added. The aqueous layer was extracted with EtOAc (3×10 ml), and the organic layer was discarded. The aqueous layer was acidified to pH 1 with conc. HCl, and extracted with EtOAc (3×10 ml). The combined organic layers were dried (MgSO4), filtered, and the solvent removed in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662839B2
Source datasetuspto-grants-2010_02
ORD IDord-d72fd24f65e3444bb06c7fd38ea172d6
Source noteuspto-grants-2010_02