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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156315생성일: 2026년 10월 25일

Water → (1-Benzylpiperidin-4-yl)(2-methylphenyl)methanone

https://huagongshe.com/reaction/1156315

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-BromotolueneHCID 7236—
반응물Ammonium ChlorideHCID 25517—
반응물1-Benzylpiperidine-4-carbonitrileHCID 793383—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물(1-Benzylpiperidin-4-yl)(2-methylphenyl)methanoneHCID 20530712—

반응 조건

온도10 °C

반응 단계

To 7 parts of magnesium is added dropwise a solution of 50 parts of 1-bromo-2-methylbenzene in 140 parts of 1,1'-oxybisethane so that the mixture is refluxing. The whole is stirred for 15 minutes at reflux. The Grignard-complex is cooled to 10° C. and there is added dropwise a solution of 36 parts of 1-(phenylmethyl)-4-piperidinecarbonitrile in 70 parts of 1,1'-oxybisethane. Upon completion, stirring is continued for 4 hours at room temperature. The reaction mixture is decomposed with a solution of 40 parts of ammonium chloride in 400 parts of water. The organic phase is separated, dried, filtered and evaporated, yielding 31 parts of (2-methylphenyl) [1-(phenylmethyl)-4-piperidinyl]methanone as an oily residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04335127
출처 데이터셋uspto-grants-1982_06
ORD IDord-a396fa39fa0a4d01b260984bec0b0da4
출처 메모uspto-grants-1982_06