Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 22221473 | HCID 22221473 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9903577 | HCID 9903577 | 103.5% |
Reaction Steps
To a solution of methyl 3-[5-(3,4-dichlorophenyl)-4-isoxazolyl]propionate (1.63 g) in tetrahydrofuran (25 ml) was gently added diisobutylaluminum hydride (1.0 M hexane solution, 13 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-(3,4-dichlorophenyl)-4-isoxazolyl]propan-1-ol (1.53 g, yield 97%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 66–67° C.
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-43d2d07a0a42429b9e46f295ab6d6426 |
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| Source note | uspto-grants-2006_04 |
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