HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-thioxopropionic acid | HCID 15158173 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acid | HCID 53679428 | 69.8% |
Reaction Steps
A mixture of 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-2-thioxopropionic acid (3.74 g), hydroxylamine hydrochloride (2.63 g), 85% potassium hydroxide (2.50 g) and 80% aqueous ethanol (22.4 ml) was refluxed for 3 hours. After cooling, to the reaction mixture was added water (40 ml) and the resulting precipitates were filtered off. The filtrate was washed with methylene chloride (20 ml) twice, acidified with 10% aqueous hydrochloric acid (pH≈2), and extracted with ethyl acetate (20 ml) twice. The organic layer was washed with water (10 ml) and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was removed to give 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acid (2.60 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155114 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-acd8396db8fa4c719e29254af4576e6f |
| Source note | uspto-grants-1992_10 |