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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 555233Erstellt: 24. Oktober 2026

1-Hydroxypiperidine → 2-Benzylpiperidin-1-ol

https://huagongshe.com/de/reaction/555233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxypiperidineHCID 20935—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178418336HCID 178418336—
KatalysatorManganese dioxideHCID 14801—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Benzylpiperidin-1-olHCID 2291158433%

Reaktionsschritte

Activated MnO2 (1.29 g, 14.8 mmol) was added to a solution of N-hydroxypiperidine (0.50 g, 4.95 mmol) in dichloromethane (25 mL) at 0° C. and the mixture was stirred for 1 h. The reaction mixture was filtered through a pad of Celite™ and Na2SO4. The filtrate was added dropwise to a solution of benzylmagnesium chloride (2.0 M in tetrahydrofuran, 4.95 mL, 9.90 mmol) at −10° C. The reaction mixture was stirred at 0° C. for 0.5 h and then saturated aqueous ammonium chloride solution (25 mL) and dichloromethane (25 mL) were added. The aqueous phase was separated and extracted with dichloromethane (2×30 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The crude product was subjected to flash chromatography on SiO2 eluting with 60% diethyl ether in hexanes to give the title compound (0.309 g, 33%) as a white crystalline solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053432B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-6366ab04bbc04550929f80c79bd779e4
Quellennotizuspto-grants-2011_11