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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706230Generated: November 1, 2026

Hydrochloric Acid → 2-hydroxy-3-(N-hydroxy-N-thienylacetylamino)propylphosphonic acid

https://huagongshe.com/reaction/1706230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantSodium BicarbonateHCID 516892—
Reactant2-hydroxy-3-(N-hydroxyamino)propylphosphonic acidHCID 13961619—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-hydroxy-3-(N-hydroxy-N-thienylacetylamino)propylphosphonic acidHCID 20337236100%

Reaction Steps

2-Hydroxy-3-(N-hydroxyamino)propylphosphonic acid (342 mg) was dissolved in a mixture of water (7 ml) and methanol (3 ml). To the solution was added dropwise thienyl acetyl chloride (385 mg) with stirring under ice-cooling, while maintaining the solution at pH 7.2-7.4 with 5% aqueous sodium bicarbonate solution. After the reaction mixture was stirred under ice-cooling for 1.5 hours, the mixture was adjusted to pH 10 with 1 N aqueous sodium hydroxide solution, and stirred under ice-cooling for 2 hours and at ambient temperature for 3 hours. Subsequently, the resultant mixture was adjusted to pH 4.0 with 1N hydrochloric acid, washed with diethyl ether (40 ml) and concentrated under reduced pressure. To the residue was added methanol to give insoluble materials, which was removed by filtration. The filtrate was concentrated under reduced pressure. To the residue was added ethanol (20 ml) and the mixture was stirred at ambient temperature for an hour to give precipitates, which were separated by filtration and dried to give powdery 2-hydroxy-3-(N-hydroxy-N-thienylacetylamino)propylphosphonic acid (0.59 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206156
Source datasetuspto-grants-1980_06
ORD IDord-211b4725573a4a6195fa2565d2e77a00
Source noteuspto-grants-1980_06