Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Sodium sulfate decahydrate | HCID 62649 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Edukt | Ethyl 5-(difluoromethoxy)picolinate | HCID 68430338 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Pyridinemethanol, 5-(difluoromethoxy)- | HCID 68431756 | 87% |
Reaktionsschritte
A toluene solution (13.8 mL, 13.8 mmols) of 1N diisobutylaluminium hydride was added to a THF solution (40 mL) of 2-ethoxycarbonyl-5-difluoromethoxypyridine (1.0 g, 4.6 mols) and stirred at 0° C. for 40 minutes. Successively sodium borohydride (174 mg, 4.6 mmols) and methanol (2 mL) were added and stirred at 0° C. for 30 minutes. Sodium sulfate decahydrate was added to the reaction liquid and stirred overnight at room temperature. Filtering the insoluble matter with Celite, the solvent was concentrated under reduced pressure. The residue was purified on silica gel column chromatography (C-300, hexane:ethyl acetate=3:2-2:3) to provide the title compound (738 mg, 87%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732456B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-2b2063a5771f49eaa882928ed87a2712 |
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| Quellennotiz | uspto-grants-2010_06 |
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