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HRID 26061作成日:2026年10月26日

Ammonium Chloride → 1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]3-hydroxypiperidine

https://huagongshe.com/reaction/26061

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
反応物MagnesiumHCID 5462224—
反応物2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzeneHCID 12882164—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]3-hydroxypiperidineHCID 1557155667%

反応条件

温度-10 °C

反応手順

A solution of 20.0 g. (51.4 mmols) of 1-bromo-2-benzyloxy-4-(1,1-dimethylheptyl)benzene in 75 ml. of tetrahydrofuran is slowly added to 2.5 g. (103 mmols) of 70-80 mesh magnesium metal. The resulting mixture is refluxed for 20 minutes and is then cooled to -10° C. A solution of 9.71 g. (51.4 mmols) of N-benzyl-3-piperidone in 25 ml. of tetrahydrofuran is then added at such a rate that the reaction temperature is maintained below 0° C. The reaction mixture is stirred for 30 minutes following completion of addition and is then added to 500 ml. of saturated ammonium chloride and 500 ml. of ether. The ether extract is washed with two 250 ml. portions of sodium chloride, dried over magnesium sulfate and evaporated to an oil. The oil is purified via column chromatography on 700 g. of silica gel eluted with 50% ether-cyclohexane to yield 17.1 g. (67%) of the title compound as an oil:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147872
出典データセットuspto-grants-1979_04
ORD IDord-d3b0b30d01ba40e3b9277c3e36967dd2
出典メモuspto-grants-1979_04