HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506301Generated: October 30, 2026
Hydroxyamine hydrochloride → HCID 136350288, compound
https://huagongshe.com/reaction/1506301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 72213375 | HCID 72213375 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136350288 | HCID 136350288 | 87% |
Reaction Steps
To 3-phenyl-4-(trifluoromethyl)isoxazole-5-carbaldehyde (Intermediate I-12B, 0.38 g, 1.576 mmol) in ethanol (5 mL) were sequentially added hydroxylamine hydrochloride (0.131 g, 1.891 mmol) and sodium acetate (0.155 g, 1.891 mmol) at room temperature. The reaction mixture was heated at 80° C. for 20 min. The reaction mixture was concentrated and water (10 ml) was added. A pale yellow solid separated out from solution, and was filtered, washed with water (2×5 mL) and dried overnight to yield 3-phenyl-4-(trifluoromethyl)isoxazole-5-carbaldehyde oxime (0.35 g, 1.366 mmol, 87% yield) as a pale yellow solid. 1H NMR (400 MHz, CDCl3) δ ppm 8.74 (br. s., 1H) 8.32 (s, 1H) 7.62-7.67 (m, 2H) 7.47-7.57 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216972B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e9ee85fd01ed465997cad51010b598b5 |
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| Source note | uspto-grants-2015_12 |
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