Reaktion #689364

Reaktionsgleichung

diethylazodicarboxylate toluene

1-(tert-Butoxycarbonyl)piperidin-3-ylmethanol

4′-chloro-4-hydroxybiphenyl

triphenylphosphine

→

desired compound

Ausbeute 67.0%

1-(tert-Butoxycarbonyl)-3-[(4′-chlorobiphenyl-4-yl)oxymethyl]piperidine

Ausbeute 67.0%

Lösungsmittel

water

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at room temperature for 16 hours
2. 2
   Extraktionthe mixture was extracted with ethyl acetate
3. 3
   WaschenThe extract washed with brine
4. 4
   Trocknenby drying over magnesium sulfate and evaporation of the solvent
5. 5
   SonstigePurification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=50:1->10:1)

Vorschrift

1-(tert-Butoxycarbonyl)piperidin-3-ylmethanol (323 mg, 1.50 mmol) and 4′-chloro-4-hydroxybiphenyl (307 mg, 1.50 mmol) were suspended in tetrahydrofuran (15 mL). To this suspension, triphenylphosphine (608 mg, 2.25 mmol) was added and the mixture was stirred at room temperature for 10 min. A 40% diethylazodicarboxylate/toluene solution (1.36 mL, 3.00 mmol) was then added and the mixture was stirred at room temperature for 16 hours. Subsequently, water was added and the mixture was extracted with ethyl acetate. The extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=50:1->10:1) gave 401 mg (67%) of the desired compound as a colorless powder.

Quelle