Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 22221215 | HCID 22221215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22220983 | HCID 22220983 | 93% |
Reaction Steps
To a solution of methyl 3-[5-(2,5-dichlorophenyl)-4-isoxazolyl]propionate (500 mg) in tetrahydrofuran (30 ml) was gently added diisobutylaluminum hydride (1.0 M toluene solution, 4.2 ml) 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-(2,5-dichlorophenyl)-4-isoxazolyl]propan-1-ol (420 mg, yield 93%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). NMR (CDCl3) δ: 1.28 (1H, t, J=5 Hz), 1.7–1.9 (2H, m), 2.5–2.6 (2H, m), 3.65 (2H, td, J=6, 5 Hz), 7.35–7.5 (3H, m), 8.27 (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-abed9e327acd48c5b4c316069aa9ff2d |
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| Source note | uspto-grants-2006_04 |
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