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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-hydroxy-3-(N-hydroxyamino)propylphosphonic acid | HCID 13961619 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-hydroxy-3-(N-hydroxy-N-thienylacetylamino)propylphosphonic acid | HCID 20337236 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04206156 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-211b4725573a4a6195fa2565d2e77a00 |
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| Source note | uspto-grants-1980_06 |
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