Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469447Generated: October 29, 2026

Sodium Hydroxide → HCID 58557018, compound

https://huagongshe.com/reaction/469447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl bromophenylacetateHCID 97780—
Reactant2-Acetyl-3-aminothiopheneHCID 2735233—
SolventAcetonitrileHCID 6342—
ProductHCID 58557018HCID 5855701834.1%

Reaction Steps

A solution of ethyl 2-bromo-2-phenylacetate (349 μl, 2.00 mmol) and 1-(3-aminothiophen-2-yl)ethanone (282 mg, 2.00 mmol) in acetonitrile (2 ml) was heated under microwave irradiation at 100° C. for 1 hour. Acetonitrile was evaporated, and the residue was dissolved in EtOH (2 ml), and sodium hydroxide (80.0 mg, 2.00 mmol) was added. The reaction mixture was stirred at room temperature for 24 hours, and then ethanol was evaporated under vacuum. The residue was taken up with water and washed with EtOAc. The pH of the aqueous phase was adjusted to 3 with HCl, and the aqueous phase was back-extracted with EtOAc. The organic phase was dried over Na2SO4, filtered and evaporated to dryness to obtain 2-(2-acetylthiophen-3-ylamino)-2-phenylacetic acid (188 mg, 34% yield), which was used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629160B2
Source datasetuspto-grants-2014_01
ORD IDord-c72d84c2171b4c7c86332128a3b6233d
Source noteuspto-grants-2014_01