Reaktion #54469

Reaktionsgleichung

3,4-dihydro-1(2H)-naphthalenone

formalin

sodium hydrogen carbonate

1-benzhydrylpiperazine hydrochloride

→

2-(4-benzhydryl-1-piperazinylmethyl)-3,4-dihydro-1(2H)-naphthalenone

Lösungsmittel

water

diethyl ether

water

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONa mixture of 10 g
2. 2
   workup.ADDITIONTo this reaction mixture is added 500 ml
3. 3
   Extraktionextracted with chloroform
4. 4
   TrocknenThe extract is dried over anhydrous sodium sulfate
5. 5
   workup.DISTILLATIONdistilled under reduced pressure
6. 6
   Sonstigeto remove the solvent

Vorschrift

In 100 ml. of ethanol is dissolved a mixture of 10 g. of 3,4-dihydro-1(2H)-naphthalenone, 22 g. of 1-benzhydrylpiperazine hydrochloride and 10 g. of 37% aqueous formalin and the mixed solution is stirred at room temperature for 3 hours and, then, heated at 80° C. for another 3 hours. To this reaction mixture is added 500 ml. of water and, after shaking with 100 ml. of diethyl ether, the water layer is neutralized with sodium hydrogen carbonate and extracted with chloroform. The extract is dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. By the above procedure is obtained an oil of 2-(4-benzhydryl-1-piperazinylmethyl)-3,4-dihydro-1(2H)-naphthalenone. This product is dissolved in a mixture of 50 ml. of chloroform and 100 ml. of methanol. After addition of 5 g. of sodium borohydride, the mixture is stirred at room temperature for 30 minutes. Following addition of 500 ml. of water, the reaction mixture is extracted with chloroform and the extract is dried. The solvent is distilled off under reduced pressure and the residue is purified by chromatography on a column of silica gel (acetone-benzene=1:9). By the above procedure is obtained 4.3 g. of 2-(4-benzhydryl-1-piperazinylmethyl)-1,2,3,4-tetrahydro-1-naphthalenol as colorless prisms melting at 179°-181° C.

Quelle