HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850293Generated: October 30, 2026
Ethanone, 2-(4-chlorophenyl)-1-phenyl- → HCID 85675368, compound
https://huagongshe.com/reaction/850293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanone, 2-(4-chlorophenyl)-1-phenyl- | HCID 95829 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 85675368 | HCID 85675368 | 92% |
Reaction Steps
To a solution of 2-(4-chlorophenyl)-1-phenyl-1-ethanone (2, 1.93 g, 8.37 mmol) in 25 ml pyridine (dried over molecular sieves) under nitrogen was added at room temperature methoxylamine hydrochloride (873 mg, 10.5 mmol). The resulting slightly cloudy, pale orange mixture was stirred at room temperature overnight. The pyridine was removed in vacuo with heating. The residual solids were stirred with ether (60 ml), isolated by filtration, and discarded. The filtrate was dried over sodium sulfate, and concentrated in vacuo to give a mixture of the oxime geometrical isomers as 2.00 g of a clear, pale yellow syrup (92% yield). 1H NMR showed the isomers to be formed in a 5:3 ratio: Rf 0.64, 0.50; IR (CDCl3) 3068 (w), 2940 (m), 2819 (w), 1602 (w), 1493 (s), 1442 (m); 1H NMR (CDCl3) 7.63 (m, 2H), 7.37-7.11 (m, 11.5 H), 4.12 (s, 2H), 4.05 (s, 3H), 3.91 (s, 1.6H), 3.82 (s, 1.2H); low resolution mass spec. 259 (M+, 8), 227 (100), 192 (28), 165 (18), 134 (12), 125 (62), 119 (37).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017910 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-92098f08b7534645a60231142a86b7a4 |
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| Source note | uspto-grants-2000_01 |
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