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HRID 1030152作成日:2026年10月26日

Sodium Chloride → 4-(4-Methoxybenzylthio)-1-methylpiperidine

https://huagongshe.com/reaction/1030152

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Sodium hydrideHCID 24758—
反応物4-Methoxy-alpha-toluenethiolHCID 80407—
反応物1-Methylpiperidin-4-yl methanesulfonateHCID 4190681—
溶媒DimethylformamideHCID 6228—
生成物4-(4-Methoxybenzylthio)-1-methylpiperidineHCID 19797259—

反応手順

10.9 ml of 4-methoxybenzyl mercaptan were dissolved in 55 ml of dry dimethylformamide, and 3.4 g of sodium hydride (as a 55% w/w suspension in mineral oil) were added to the solution, whilst ice-cooling. The mixture was then stirred at room temperature for 30 minutes. At the end of this time, a solution of 12.6 g of 4-methanesulfonyloxy-1-methylpiperidine in 63 ml of dry dimethylformamide was added to the mixture, which was then allowed to stand overnight at room temperature. The reaction mixture was then poured into an aqueous solution of sodium chloride and extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel (eluted with a 1:4 by volume mixture of ethyl acetate and methanol) to afford 9.01 g of the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05104867
出典データセットuspto-grants-1992_04
ORD IDord-76c33d94782249f4960c9fc225f7d462
出典メモuspto-grants-1992_04