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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 538661Erstellt: 25. Oktober 2026

Benzyl Bromide → (1-Benzylpiperidin-2-yl)methanol

https://huagongshe.com/reaction/538661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
EduktPiperidin-2-ylmethanolHCID 94263—
LösungsmittelDimethylformamideHCID 6228—
Produkt(1-Benzylpiperidin-2-yl)methanolHCID 2735486—

Reaktionsschritte

To a stirred solution of piperidine-2-methanol (12; 6 g, 52.09 mmol) in dimethylformamide (DMF, 50 mL) were added successively K2CO3 (10.78 g, 78.14 mmol) and benzyl bromide (6.85 mL, 57.30 mmol) at 0° C. and the mixture stirred at rt for 16 hours. The reaction mixture was then filtered and the filtrate was concentrated. The residue was dissolved in EtOAc and the organic layer was washed with water and brine solution. The organic layer was dried over Na2SO4, filtered and concentrated. The crude material was purified by chromatography on 230-400 mesh silica gel eluting with 30% EtOAc-hexane to provide compound 13.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865741B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-f3b5f33e2aa04103be774d913a3b03ab
Quellennotizuspto-grants-2014_10