HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897464Generated: October 26, 2026
4-Bromobenzophenone → Methanone, (4-bromophenyl)phenyl-, oxime
https://huagongshe.com/reaction/897464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzophenone | HCID 7030 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methanone, (4-bromophenyl)phenyl-, oxime | HCID 3484095 | 94% |
Reaction Steps
A mixture of 4-bromobenzophenone (10.0 g, 0.0383 mol) and hydroxylamine hydrochloride (13.3 g, 0.192 mol) was heated in a mixture of ethanol (250 mL) and pyridine (50 mL) at reflux for 2 hours under an atmosphere of nitrogen. The solvents were removed under the reduced pressure and the residue was partitioned between water (300 mL) and dichloromethane (300 mL). The water phase was further extracted with dichloromethane twice (180 mL each) and the combined organic extracts were dried over magnesium sulfate. The solvent was removed under the reduced pressure and the residue was purified by flash chromatography on silica gel using ethyl acetate/n-heptane (1:9) as mobile phase to yield (4-bromophenyl)(phenyl)methanone oxime as a white solid (9.93 g, 0.036 mol): 1H NMR (DMSO-d6, 400 MHz) 7.66 (d, 1H), 7.57(d, 1H), 7.33 (m, 7H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-465b726311b6481b98bef0f2a57db009 |
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| Source note | uspto-grants-2005_07 |
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