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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 451673Erstellt: 24. Oktober 2026

(R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate → 2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanol

https://huagongshe.com/de/reaction/451673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylateHCID 59201708—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanolHCID 59201741—

Reaktionsschritte

A solution of crude (R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate in CH3CN (100 mL) and 2 N aq HCl (100 mL) was vigorously stirred at rt for 2 d. The solvents were removed in vacuo to give the HCl salt of 2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanol, which was used in the next step without further purification. LC-MS (3 min) tR=1.05 min m/z 272, 270 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08487108B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-5b404a4e2a6445a599aa7c2199b939f4
Quellennotizuspto-grants-2013_07