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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1720444Erstellt: 27. Oktober 2026

3-Pyridinecarboxaldehyde → Pyridin-3-yl(thiophen-2-yl)methanol

https://huagongshe.com/reaction/1720444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PyridinecarboxaldehydeHCID 10371—
EduktChloroform methanolHCID 21584188—
EduktHCID 178418439HCID 178418439—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPyridin-3-yl(thiophen-2-yl)methanolHCID 65049962,2%

Reaktionsbedingungen

Temperatur-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05506261
Quelldatensatzuspto-grants-1996_04
ORD IDord-8f9a716072bd4c0bb8c2d6b1c9629c25
Quellennotizuspto-grants-1996_04