HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060749Generated: October 29, 2026
Hydroxyamine hydrochloride → HCID 76540720, compound
https://huagongshe.com/reaction/2060749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(Allyloxy)-1-(5-bromo-2-fluorophenyl)ethanone | HCID 57475762 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 76540720 | HCID 76540720 | — |
Reaction Steps
To a solution of 2-(allyloxy)-1-(5-bromo-2-fluorophenyl)ethanone (118 g, 432.1 mmol) in ethanol (1.7 L) is added hydroxylamine hydrochloride (34.5 g, 496.9 mmol) and sodium ethanoate (40.8 g, 496.9 mmol) at 25° C. The reaction is heated at 70° C. for 1 hr. The reaction is cooled and the solvent is removed under reduced pressure. The residue is washed with water (1 L) and is extracted three times with dichloromethane (3×500 mL). The organic phase is dried over magnesium sulfate, filtered, and the solvent is removed under reduced pressure, to obtain the title compound as a mixture of two possible oximes (120 g, 96%). ES/MS m/e (79Br/81Br) 288, 290 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278441B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-83adc85bc82e4ca2ac37e0fc8bc1e496 |
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| Source note | uspto-grants-2012_10 |
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