Reacción #78239

Ecuación de reacción

sodium bicarbonate

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

4-n-butoxyaniline

Phosphorous oxychloride

→

titled compound

Rendimiento 24.0%

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

Rendimiento 24.0%

Disolventes

methylene chloride

pyridine

Condiciones de reacción

Tratamiento posterior

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

Procedimiento

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).

Fuente