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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324544Erstellt: 24. Oktober 2026

Water → 1-Benzyl-3-phenyl-piperidin-3-ol

https://huagongshe.com/de/reaction/324544

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTetrahydrofuranHCID 8028—
Edukt3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
EduktHCID 178418255HCID 178418255—
LösungsmittelTolueneHCID 1140—
Produkt1-Benzyl-3-phenyl-piperidin-3-olHCID 33912880%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1-benzyl-3-piperidinone (0.193 g, 1.02 mmol) in toluene dry (10 mL) cooled at 0° C. was added a solution of phenyl magnesium bromide 3.1M in THF (0.48 mL, 1.4 mmol). The resulting solution was maintained at 0° C. for 2 h, then was allowed to warm at 25° C. for 1 h. Water (50 mL) was added and the mixture was extracted with EtOAc (2×50 mL). The collected organic phase was dried and concentrated under reduced pressure. The crude compound was purified by flash chromatography on silica gel using EtOAc/cyclohexane as eluant to afford the title compound as a white solid (0.235 g, 80%). 1H NMR (CDCl3): 1.65-1.85 (m, 3H), 1.9-2.15 (m, 1H), 2.067 (bd, J=8.1 Hz, 1H), 2.34 (d, J=11.1 Hz, 1H), 2.77 (d, J=11.1 Hz, 1H), 2.95 (bd, J=8.1 Hz, 1H), 3.60 (s, 2H), 4.005 (bs, 1H), 7.2-7.4 (m, 8H), 7.50 (s, 1H), 7.525 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218404B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-85f8712dce0a4789a3775707b50bbda7
Quellennotizuspto-grants-2001_04