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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397215Generated: November 2, 2026

Hydroxyamine hydrochloride → 2-(Hydroxyimino)-3-(4-phenylthiophen-2-yl)propanoic acid

https://huagongshe.com/reaction/1397215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-(4-Phenylthiophen-2-yl)-2-thioxopropanoic acidHCID 86677588—
SolventSodium ethoxideHCID 2723922—
Product2-(Hydroxyimino)-3-(4-phenylthiophen-2-yl)propanoic acidHCID 8667758990%

Reaction Steps

3-(4-Phenylthiophen-2-yl)-2-thioxopropanoic acid (0.9 g, 3.4 mmol), hydroxylamine hydrochloride (740 mg, 10.6 mmol), and an ethanolic solution sodium ethoxide [prepared from 0.4 g of sodium and 30 mL of absolute ethanol] was refluxed for 1.5 h. Solvent was removed under reduced pressure and the residue was diluted with water and acidified with 1.5N HCl to adjust the pH of the solution ˜3. The solid product was extracted with EtOAc. The organic layer was dried over anhydrous Na2SO4, then removal of the solvent under reduced pressure yielded 2-(hydroxyimino)-3-(4-phenylthiophen-2-yl)propanoic acid (0.8 g, yield 89%) as an off-white solid. 1H NMR (400 MHz, MeOD) δ 7.59-7.57 (m, 2H), 7.37-7.33 (m, 3H), 7.24-7.23 (m, 2H), 3.31 (s, 2H). MS (ESI) m/z: Calculated for C13H11NO3S: 262.05. found: 262.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-8aa348a7d3944d9b91de0b3f0ae05967
Source noteuspto-grants-2014_12