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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 412512Erstellt: 25. Oktober 2026

1-(Pyridin-4-yl)piperidine-4-carboxylic acid → (1-(Pyridin-4-YL)piperidin-4-YL)methanol

https://huagongshe.com/reaction/412512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Pyridin-4-yl)piperidine-4-carboxylic acidHCID 1268289—
EduktBorane;tetrahydrofuranHCID 2723981—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(1-(Pyridin-4-YL)piperidin-4-YL)methanolHCID 11310048—

Reaktionsschritte

Under an argon atmosphere, to a solution of 1-(pyridin-4-yl)piperidine-4-carboxylic acid (Tetrahedron, vol. 44, No. 23, page 7095 (1988)) (500 mg) in tetrahydrofuran (5 ml) was added 1M borane-tetrahydrofuran solution (14.5 ml) with ice-cooling, and the mixture was stirred at room temperature for 12 hours. After completion of the reaction, the reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in 12% hydrochloric acid and stirred at 50° C. for 1 hour. The reaction mixture was neutralized with aqueous sodium hydrogencarbonate and 4N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and dried under reduced pressure to give the title compound (400 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06562828B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-2323eb6dea95474aa3ed3d573ce4b9e2
Quellennotizuspto-grants-2003_05