HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 914456Erstellt: 26. Oktober 2026
Sodium Hydroxide → (6-Phenylpyridin-3-yl)methanol
https://huagongshe.com/reaction/914456
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Sodium Sulfate | HCID 24436 | — |
| Edukt | Ethyl 6-phenylnicotinate | HCID 11096332 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (6-Phenylpyridin-3-yl)methanol | HCID 22254216 | 99,3% |
Reaktionsschritte
Lithium aluminum hydride (3.50 g) was suspended in tetrahydrofuran (200 mL), 6-phenylnicotinic acid ethyl ester (21.0 g) synthesized in Reference Example 19 was added under ice-cooling, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was ice-cooled, water (5 mL) and aqueous sodium hydroxide solution (1 mol/L, 10 mL) were successively added dropwise. After warming to room temperature, the mixture was stirred for 1 hr. Anhydrous sodium sulfate was added to the reaction mixture, the mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate=1:1 to 1:3) to give the title compound (17.0 g) as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08026370B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-b291f32fafb14751874c9cbdacd2d01c |
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| Quellennotiz | uspto-grants-2011_09 |
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