Reaktion #11648

Reaktionsgleichung

sodium bicarbonate

(4-Nitro-phenyl)-acetic acid

piperidine

→

2-(4-nitro-phenyl)-1-piperidin-1-yl-ethanone

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeA room temperature solution of 2.53 gms
2. 2
   Sonstige1′,1′-carbonyl-diimidizole and immediately immersed in an ice bath
3. 3
   Extraktionthe resulting mixture is extracted with ethyl acetate
4. 4
   SonstigeThe organics are separated
5. 5
   Trocknendried over anhydrous sodium sulfate
6. 6
   Filtrationfiltered
7. 7
   Sonstigesubsequently evaporated to dryness in vacuo
8. 8
   SonstigeThe crude product residue is then chromatographed by flash silica gel chromatography
9. 9
   Sonstigeevaporation of solvent

Vorschrift

A room temperature solution of 2.53 gms. (4-Nitro-phenyl)-acetic acid in tetrahydrofuran (10 mL) is treated with 2.44 gms. 1′,1′-carbonyl-diimidizole and immediately immersed in an ice bath. The reaction mixture is stirred in the ice bath for 30 minutes then it is allowed to warm to room temperature. Once at room temperature the reaction mixture is treated with 1.21 mL piperidine, and then is stirred overnight at room temperature. The reaction is then made basic with the addition of saturated aqueous sodium bicarbonate, and the resulting mixture is extracted with ethyl acetate. The organics are separated, dried over anhydrous sodium sulfate, filtered, and subsequently evaporated to dryness in vacuo. The crude product residue is then chromatographed by flash silica gel chromatography using 50% ethyl acetate in hexanes as the eluant. Following evaporation of solvent, 2-(4-nitro-phenyl)-1-piperidin-1-yl-ethanone is isolated as a white solid in the amount of 3.18 gms.

Quelle