Reaktion #78239

Reaktionsgleichung

sodium bicarbonate

(1-benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium salt

4-n-butoxyaniline

Phosphorous oxychloride

→

titled compound

Ausbeute 24.0%

N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide

Ausbeute 24.0%

Lösungsmittel

methylene chloride

pyridine

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionthe solution was extracted with ethyl acetate
2. 2
   WaschenThe organic layer was washed with water and saturated brine
3. 3
   Trocknendried over anhydrous sodium sulfate
4. 4
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
5. 5
   SonstigeThe residue was purified with silica gel column chromatography (elution solvent; methylene chloride:methanol=19:1 to 9:1)

Vorschrift

To a solution of (1-benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium salt (3.09 g) in methylene chloride (60 mL) were added 4-n-butoxyaniline (2.0 g) and pyridine (2.14 mL). Phosphorous oxychloride (1.19 mL) was added dropwise to the solution under cooling with an ice-sodium chloride, followed by stirring at 5 to 10° C. for 1 hour. The mixture was made alkaline with saturated aqueous sodium bicarbonate under cooling with an ice-water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate, and then, the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography (elution solvent; methylene chloride:methanol=19:1 to 9:1) to obtain the titled compound (1.15 g).

Quelle