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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33533Erstellt: 26. Oktober 2026

Sodium borohydride → (5-(4-Chlorophenyl)pyridin-3-yl)methanol

https://huagongshe.com/reaction/33533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
EduktMethyl 5-(4-chlorophenyl)nicotinateHCID 20099851—
LösungsmittelEthanolHCID 702—
Produkt(5-(4-Chlorophenyl)pyridin-3-yl)methanolHCID 2472985368,1%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 900 mg (3.49 mmol) 5-(4-Chloro-phenyl)-nicotinic acid methyl ester in 30.0 ml Ethanol was treated at room temperature (r. t.) with 264 mg (69.9 mmol) of sodium borohydride. The mixture was stirred for two days at 50° C. Then it was poured on ice and extracted tree times with ethyl acetate. The combined organic phases were washed with water, dried (sodium sulphate) and evaporated. Chromatography on silica (eluent: ethyl acetate/methanol 6:1) gave 522 mg (67%) of [5-(4-Chloro-phenyl)-pyridin-3-yl]-methanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429605B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-f884a7a13b014bd7be0032f745530dc0
Quellennotizuspto-grants-2008_09