Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 22221082 | HCID 22221082 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22221203 | HCID 22221203 | 68.1% |
Reaction Steps
To a solution of methyl 3-[5-(2,4-difluorophenyl)-4-isoxazolyl]propionate (1.05 g) in tetrahydrofuran (30 ml) was gently added diisobutylaluminum hydride (1.0 M hexane solution, 8.7 ml) at 0° C., and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into dilute hydrochloric acid, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 3-[5-(2,4-difluorophenyl)-4-isoxazolyl]propan-1-ol (640 mg, yield 68%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). NMR (CDCl3) δ: 1.29 (1H, br s), 1.75–1.95 (2H, m), 2.55–2.65 (2H, m), 3.6–3.75 (2H, m), 6.9–7.1 (2H, m), 7.5–7.65 (1H, m), 8.25 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022725B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-9052a72f267445188ed4789622ba0885 |
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| Source note | uspto-grants-2006_04 |
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