Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Butyn-2-ol | HCID 16239 | — |
| Reactant | N-[(4-fluorophenyl)methylidene]hydroxylamine | HCID 68017 | — |
| Reactant | N-chlorosuccinamide | HCID 15238416 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86680476 | HCID 86680476 | 51.7% |
Reaction Steps
To a stirred solution of 4-fluorobenzaldehyde oxime (0.2 g, 1.4 mmol) in DCM (10 mL) was added N-chlorosuccinamide (0.1 g, 1.4 mmol) and the reaction stirred for 1 hour at room temperature. But-3-yn-2-ol (0.23 g, 1.68 mmol) was added and the reaction mixture stirred at reflux for 3 h. After completion of the reaction (as monitored by TLC), the mixture was extracted with DCM (3×100 mL), the organic layer washed with water (100 mL) followed by brine (100 mL), dried over sodium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (60-120 mesh; using 50% ethyl acetate in hexanes) to obtain 1-(3-(4-fluorophenyl)isoxazol-5-yl)ethanol as liquid (0.15 g, 50% yield). 1H NMR (400 MHz, CDCl3): δ 7.76 (dd, 2H), 7.05 (t, 2H), 6.48 (s, 1H), 5.04 (q, 1H), 1.63 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809372B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-01a4987bddd2429d9173d23709d0c070 |
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| Source note | uspto-grants-2014_08 |
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