HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52182Erstellt: 26. Oktober 2026
3-Pyridinecarboxaldehyde → Pyridin-3-yl(thiophen-2-yl)methanol
https://huagongshe.com/reaction/52182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Edukt | Chloroform methanol | HCID 21584188 | — |
| Edukt | HCID 178418439 | HCID 178418439 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Pyridin-3-yl(thiophen-2-yl)methanol | HCID 650499 | 62,2% |
Reaktionsschritte
To a solution of 3-pyridinecarboxaldehyde (5.0 mL, 53 mmol) in THF at -78° C. was added 2-thienyllithium (1.0M in THF. 64 mL, 64 mmol) and the reaction mixture was stirred for 2 hours at -78° C. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with ether. The organic phase was dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (5%, then 10% methanol/CHCl3) gave 2-(3-pyridylhydroxymethyl)thiophene (6.30 g, 62% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616596 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-821002a002e645fc8b3d520076f6a82a |
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| Quellennotiz | uspto-grants-1997_04 |
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