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HRID 962465作成日:2026年10月26日

ethyl N-(2-phenoxyethyl)piperidine-3-carboxylate → N-(2-phenoxyethyl)piperidine-3-carbaldehyde

https://huagongshe.com/reaction/962465

反応式

関与物質

役割名称HCID仕込み量
反応物ethyl N-(2-phenoxyethyl)piperidine-3-carboxylateHCID 19085394—
反応物DiisobutylaluminumhydrideHCID 21225700—
溶媒TetrahydrofuranHCID 8028—
生成物N-(2-phenoxyethyl)piperidine-3-carbaldehydeHCID 19085423—

反応手順

Di-isobutylaluminium hydride (13.2 ml of 1.5M solution in toluene) was added to a mixture of ethyl N-(2-phenoxyethyl)piperidine-3-carboxylate (5.0 g) in dry THF (50 ml) at 0° C. under nitrogen with stirring. The mixture was quenched with water (5 ml) and then treated with saturated Rochelles salt solution. The mixture was stirred at room temperature for 30 minutes and then filtered. The filtrate was separated and the organic layer was washed, dried and evaporated to give N-(2-phenoxyethyl)piperidine-3-carbaldehyde as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760035
出典データセットuspto-grants-1998_06
ORD IDord-86a32a8d7c7c4ddf816e1c1dd0855d91
出典メモuspto-grants-1998_06