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HRID 253060作成日:2026年10月27日

Water → Benzyl 4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/253060

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物Benzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Benzyl 4-methoxypiperidine-1-carboxylateHCID 2302430145%

反応手順

To a solution of 1-benzyloxycarbonyl-4-hydroxypiperidine (1.3 g) in dimethylformamide (10 mL) was added sodium hydride (360 mL) under ice cooling and the mixture was stirred at room temperature under nitrogen-gas atmosphere for 1 hours. To the reaction mixture was added methyl iodide (374 μL) under ice-cooling and the mixture was stirred at the same temperature for 1 hour and at room temperature for 2 hours. To the reaction mixture was added water and ethyl acetate and the mixture was stirred. The organic layer washed with a brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=88/12 to 70/30) to obtain 1-benzyloxycarbonyl-4-methoxypiperidine (622 mg, yield: 45%) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872006B2
出典データセットuspto-grants-2011_01
ORD IDord-e9dd1c0189ef49e99991622f5a437a99
出典メモuspto-grants-2011_01