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HRID 1801585作成日:2026年10月25日

Dimethyl Sulfoxide → Methyl 1-(4-formyl-2-nitrophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1801585

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Cesium carbonateHCID 10796—
反応物4-Chloro-3-nitrobenzaldehydeHCID 85505—
反応物Methyl isonipecotateHCID 424914—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 1-(4-formyl-2-nitrophenyl)piperidine-4-carboxylateHCID 911129143.7%

反応条件

温度100 °C

反応手順

To a mixture of 4-chloro-3-nitrobenzaldehyde 57 (5.099 g, 27 mmol), cesium carbonate (9.48 g, 29 mmol), and methyl piperidine-4-carboxylate (4 mL, 27 mmol) was added DMSO (27 mL). The reaction mixture was heated to 100° C. for 30 min and diluted with EtOAc. The organic phase was washed with water (2×), brine (1×), dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 30% to 50% EtOAc in hexanes) gave methyl 1-(4-formyl-2-nitrophenyl)piperidine-4-carboxylate 58 (3.45 g, 43% yield) as a yellow oil. Mass spectrum: calculated for C14H16N2O5 292.1. found 293.1 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08349831B2
出典データセットuspto-grants-2013_01
ORD IDord-6a1c2fc5105048648d90d137b877ecb4
出典メモuspto-grants-2013_01