Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 12043169 | HCID 12043169 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 85074082 | HCID 85074082 | 85.7% |
Reaction Steps
A stirred mixture of 4-[4-(5-chloro-thiophen-2-yl)-phenyl]-4-oxo-butyric acid (0.065 g, 0.00022 mol), hydroxylamine hydrochloride (0.0181 g, 0.000260 mol), sodium carbonate (0.0280 g, 0.000260 mol), and absolute ethanol was refluxed under nitrogen for 17 hours and allowed to cool. The resulting suspension was stirred at room temperature for 2 days and filtered. The filtercake was dissolved in methanol (5 mL) and water (5 mL), and the solution was filtered to remove a small amount of fines. The filtrate was acidified with 1.0 M aqueous hydrochloric acid (0.24 mL, 0.00024 mol), and the resulting suspension was rotary evaporated to remove methanol. The resulting aqueous suspension was filtered, washed with water, and dried in vacuo to give 0.0584 g of 4-[4-(5-chloro-thiophen-2-yl)-phenyl]-4-hydroxyimino-butyric acid as a pale yellow solid; mp 172-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399612B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-fffe887a42024f9bbda9c0ff8f122cb6 |
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| Source note | uspto-grants-2002_06 |
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