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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606156Erstellt: 25. Oktober 2026

Water → 2-(1-Benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanol

https://huagongshe.com/reaction/606156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Bromo-2-chlorobenzeneHCID 12754—
Edukt4-Piperidineacetaldehyde, 1-(phenylmethyl)-HCID 10013602—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(1-Benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanolHCID 22248584—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

After dissolving 1.75 ml of 1-bromo-2-chlorobenzene in 30 ml of tetrahydrofuran, the solution was cooled to −78° C. Next, 5.31 ml of n-butyllithium (2.6 M, n-hexane solution) was added dropwise thereto while stirring and after 1 hour, a solution of 2.50 g of 1-benzylpiperidine-4-acetaldehyde in tetrahydrofuran (10 ml) was added and stirring was continued for 1 hour. After adding water to the reaction solution, the temperature was raised to room temperature and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 2-(1-benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915274B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-08da84c0378748d1ad2defc78b07a4fd
Quellennotizuspto-grants-2011_03