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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1389870생성일: 2026년 10월 26일

Diethyl Ether → 8-Methyl-1-naphthyl 4-piperidyl ketone hydrochloride

https://huagongshe.com/reaction/1389870

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Ammonium ChlorideHCID 25517—
반응물1-Acetylpiperidine-4-carbonitrileHCID 2756286—
반응물1-Bromo-8-methylnaphthaleneHCID 4250949—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물8-Methyl-1-naphthyl 4-piperidyl ketone hydrochlorideHCID 20295570—

반응 단계

A solution of 10.0 g (45 mmoles) of 1-bromo-8-methylnaphthalene in 5 ml of ethyl ether is added gradually to a stirred mixture of 1.2 g (50 mmoles) of magnesium in 30 ml of anhydrous ether. The mixture is stirred at reflux for 1 hour and a solution of 6.0 g (43 mmoles) of 1-acetyl-4-piperidinecarbonitrile in 10 ml of tetrahydrofuran slowly added. The mixture is allowed to stir for 16 hours, an excess of saturated aqueous ammonium chloride solution added and the mixture heated on a steam bath for 3 hours. After cooling, the mixtures is extracted with toluene and the organic phase dried over MgSO4, filtered and concentrated in vacuo. The residue is dissolved in 20 ml of ethanol and made basic with sodium hydroxide and the solution extracted into toluene. Dry hydrogen chloride is bubbled through the organic phase to yield 8-methyl-1-naphthyl 4-piperidyl ketone hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04246268
출처 데이터셋uspto-grants-1981_01
ORD IDord-80c70c83a58a47b79c299725578eccaf
출처 메모uspto-grants-1981_01