HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612811Generated: November 1, 2026
Methanol → 2-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime
https://huagongshe.com/reaction/612811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 2-Bromo-2-hydroxy-1-phenylethan-1-one | HCID 22237169 | — |
| Product | 2-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime | HCID 135980329 | 52% |
Reaction Steps
107.5 g (0.5 mol) of ω-bromo-2-hydroxy-acetophenone in 500 ml of methanol together with 41.75 g (0.5 mol) of O-methylhydroxylamine hydrochloride are heated under reflux for 4 hours. The methanol is distilled off under reduced pressure and the residue is admixed with 500 ml of water and extracted with 4 times 100 ml of ethyl acetate. The organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure. At 0° C. , the residue is stirred with petroleum ether, affording 74 g (52% of theory) of crystalline 2-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime as a mixture of two stereoisomers (53% of isomer B and 33% of isomer A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005104 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-3ee08129f065433d838fca38966f2c19 |
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| Source note | uspto-grants-1999_12 |
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