HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1620293Erstellt: 25. Oktober 2026
Sodium borohydride → (6-Methoxyquinolin-3-yl)methanol
https://huagongshe.com/reaction/1620293
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 6-Methoxyquinoline-3-carbaldehyde | HCID 12329512 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (6-Methoxyquinolin-3-yl)methanol | HCID 304667 | 49% |
Reaktionsschritte
To a stirred solution of 6-methoxyquinoline-3-carbaldehyde (1.00 g, 5.3 mmol) in THF (50 mL) in a 100 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (0.20 g, 5.3 mmol) and the mixture was stirred overnight at RT then cooled in an ice bath before quenching by addition of a 1 N aq. HCl solution (12 mL). After stirring for 15 min at RT, the mixture was basified to pH=9 with a 2 N aq. NaOH solution. THF was removed at 40° C. under vacuum and the solution was extracted with CH2Cl2 (200 mL), washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated under vacuum. Purification by column chromatography (SiO2, eluent cyclohexane:EtOAc=100:0 to 0:100) gave (6-methoxyquinolin-3-yl)methanol SLA 47088A as a yellow solid (0.49 g, 49% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08772316B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-77b919bd3e704a9498fde23658395d54 |
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| Quellennotiz | uspto-grants-2014_07 |
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