1-[3-(4-Benzyloxy-phenoxy)-propyl]-piperidine → 4-(3-Piperidin-1-yl-propoxy)-phenol

HRID 456940Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 456940
C([O:8][C:9]1[CH:24]=[CH:23][C:12]([O:13][CH2:14][CH2:15][CH2:16][N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[CH:11][CH:10]=1)C1C=CC=CC=1.C([O-])=O.[NH4+]>[Pd].CO>[N:17]1([CH2:16][CH2:15][CH2:14][O:13][C:12]2[CH:11]=[CH:10][C:9]([OH:8])=[CH:24][CH:23]=2)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]1

Komponenten

5

Reaktionsbedingungen

Temperatur
68 °C

Versuchsvorschrift

A suspension of the product of Example 6 (2.5 g), ammonium formate (2.7 g), and 10% palladium on carbon (2.5 g) in methanol (100 mL) was heated in a 68° C. bath for 3 h, and allowed to cool to room temperature. The mixture was filtered through Celite, and the filtrate was evaporated in vacuo. Saturated aqueous sodium bicarbonate was added, and the mixture was extracted with dichloromethane (4×30 mL). The combined organic phases were dried (magnesium sulfate) and evaporated in vacuo, yielding the title compound as a pink microcrystalline solid (1.3 g) which was used without further purification. A small sample (100 mg) was recrystallized (ethanol) to obtain the title compound as beige prisms (68 mg).

Aufarbeitung

  1. temperatureto cool to room temperature
  2. filtrationThe mixture was filtered through Celite
  3. customthe filtrate was evaporated in vacuo
  4. additionSaturated aqueous sodium bicarbonate was added
  5. extractionthe mixture was extracted with dichloromethane (4×30 mL)
  6. dry with materialThe combined organic phases were dried (magnesium sulfate)
  7. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-7019f0e13fe44146b980dfbcaa1bd4ef
Quelldatensatz
uspto-grants-2007_03
Patentnummer
US07186732B2

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