Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469453Generated: November 3, 2026

Phenylboronic Acid → HCID 58557000, compound

https://huagongshe.com/reaction/469453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventAcetonitrileHCID 6342—
ProductHCID 58557000HCID 5855700082%

Reaction Steps

A mixture of phenylboronic acid (286 mg, 2.35 mmol), methyl 3-aminothiophene-2-carboxylate (369 mg, 2.35 mmol), and 2-oxoacetic acid hydrate (216 mg, 2.35 mmol) in acetonitrile (20 ml) was stirred at room temperature for 2 hours. The reaction was filtered, and the precipitated was washed with little acetonitrile. The solution was concentrated under reduced pressure, and the precipitate was collected again by filtration, washing with little acetonitrile. The combined precipitates were dried under vacuum overnight to obtain 2-(2-(methoxycarbonyl)thiophen-3-ylamino)-2-phenylacetic acid (558 mg, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629160B2
Source datasetuspto-grants-2014_01
ORD IDord-4ac5e791d35f477e9179ddd7d73f9299
Source noteuspto-grants-2014_01