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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26191생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/26191

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물1-TetraloneHCID 10724—
반응물Sodium BicarbonateHCID 516892—
반응물1-Benzhydrylpiperazinium chlorideHCID 44146891—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물2-(4-benzhydryl-1-piperazinylmethyl)-3,4-dihydro-1(2H)-naphthalenoneHCID 21325000—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148897
출처 데이터셋uspto-grants-1979_04
ORD IDord-5d57ef2d0a3e4f38aa7a8a128ac0839b
출처 메모uspto-grants-1979_04