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HRID 1389870作成日:2026年10月27日

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

https://huagongshe.com/reaction/1389870

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Ammonium ChlorideHCID 25517—
反応物1-Acetylpiperidine-4-carbonitrileHCID 2756286—
反応物1-Bromo-8-methylnaphthaleneHCID 4250949—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物8-Methyl-1-naphthyl 4-piperidyl ketone hydrochlorideHCID 20295570—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04246268
出典データセットuspto-grants-1981_01
ORD IDord-80c70c83a58a47b79c299725578eccaf
出典メモuspto-grants-1981_01