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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555341Generated: October 29, 2026

Phenylboronic Acid → HCID 57948698, compound

https://huagongshe.com/reaction/555341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57948746HCID 57948746—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 57948698HCID 5794869833%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of compound 1 (7 mg, 0.018 mmol), benzeneboronic acid (2.6 mg, 0.021 mmol) and tetrakis(triphenylphosphine)palladium (2 mg, 0.002 mmol) in DMF (2 mL)/aqueous 2 N sodium bicarbonate solution (0.5 mL) is stirred for 20 minutes in a microwave reactor at 130° C. After being cooled to room temperature, the reaction mixture is extracted with ethyl acetate (3×10 mL). The combined organic phases are dried over sodium sulfate and concentrated in vacuo. The residue is subjected to flash column chromatography (silica gel, 30% EtOAc in hexanes) to afford compound 29 (2.3 mg, 33%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053442B2
Source datasetuspto-grants-2011_11
ORD IDord-410b88afe1364f3c97053ec2317d86c7
Source noteuspto-grants-2011_11