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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219871Erstellt: 24. Oktober 2026

Sodium borohydride → (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol

https://huagongshe.com/de/reaction/219871

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehydeHCID 23091101—
LösungsmittelMethanolHCID 887—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt(5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanolHCID 5855419797%

Reaktionsschritte

To a solution of 5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde (16.30 g; 57.76 mmol) in MeOH (300 mL) was added sodium borohydride (2.19 g; 57.76 mmol) at 5° C. in a portion-wise fashion and stirred for 30 min. After this time, reaction mixture was diluted with a saturated aqueous solution of NH4Cl (300 mL), extracted with EtOAc. The org layers were washed with aqueous solution of NH4Cl (150 mL), brine (300 mL), dried over MgSO4 and evaporated under vacuum to give the title compound as a yellow oil (15.9 g, 97%). LC/MS (Method A): 285.6 (M+H)+. HPLC (Method A): Rt 2.13 min (Purity: 94.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202865B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-7623db50dd62442a9174e143c5e24cd4
Quellennotizuspto-grants-2012_06