反応 #54469

反応方程式

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

formalin

sodium hydrogen carbonate

1-benzhydrylpiperazine hydrochloride

→

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

溶媒

water

diethyl ether

water

ethanol

反応条件

後処理

1. 1
   workup.ADDITIONa mixture of 10 g
2. 2
   workup.ADDITIONTo this reaction mixture is added 500 ml
3. 3
   抽出extracted with chloroform
4. 4
   乾燥The extract is dried over anhydrous sodium sulfate
5. 5
   workup.DISTILLATIONdistilled under reduced pressure
6. 6
   その他to remove the solvent

実験手順

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.

出典