Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 86695786 | HCID 86695786 | — |
| Product | HCID 87106032 | HCID 87106032 | 23% |
Reaction Steps
To a solution of ethyl (2E)-3-(6-{[4-(2-oxo-2-phenylethoxy)benzyl]oxy}pyridin-3-yl)prop-2-enoate (0.13 g, 0.3 mmol) in ethanol was added pyridine (0.038 g, 0.45 mmol) and O-Methoxylamine hydrochloride, the resulting mass was refluxed at 80° C. for 3 h. Reaction quenched with water and extracted with ethyl acetate, organic layer was washed with water and brine solution dried over anhydrous Na2SO4 and concentrated to colourless oil (0.03 g, Yield: 23%); MS (ESI, 120 eV): m/z=449 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-5b301298526f4a8088e363d6dca136bc |
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| Source note | uspto-grants-2016_03 |
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