HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104495Generated: October 30, 2026
Hydroxyamine hydrochloride → HCID 87202177, compound
https://huagongshe.com/reaction/2104495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone | HCID 11360909 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 87202177 | HCID 87202177 | 75.2% |
Reaction Steps
Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone (Example 1, 0.128 g, 0.339 mmol) was taken into EtOH/H2O (7 mL, 7:3 mixture) along with hydroxylamine hydrochloride (0.028 g, 0.407 mmol) and sodium acetate trihydrate (0.061 g, 0.447 mmol) and this mixture was refluxed for 1.5 hours. TLC and LC-MS showed no reaction. Therefore, excess quantities of hydroxylamine hydrochloride and sodium acetate trihydrate were added and refluxing was continued overnight. The reaction was concentrated and the resulting material was taken up into CH2Cl2/H2O. The layers were separated and the aqueous layer was extracted with CH2Cl2. The combined organics were dried over sodium sulfate and concentrated. The product was purified via column chromatography using 15% ethyl acetate in hexane as the eluent to afford 0.100 g of desired product as a white solid. MS (ESI) m/z 393 ([M+H]+);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576215B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-37664e904dad41e9aecd67c15757dd40 |
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| Source note | uspto-grants-2009_08 |
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