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HRID 1003678作成日:2026年10月27日

4-Ethoxybenzaldehyde → alpha-(4Ethoxyphenyl)-N-cyclopentylnitrone

https://huagongshe.com/reaction/1003678

反応式

関与物質

役割名称HCID仕込み量
反応物4-EthoxybenzaldehydeHCID 24834—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物N-cyclopentylhydroxylamineHCID 10219393—
溶媒TolueneHCID 1140—
生成物alpha-(4Ethoxyphenyl)-N-cyclopentylnitroneHCID 8658790865.1%

反応手順

4-Ethoxybenzaldehyde (22.0 g, 0.1467 mol) and N-cyclopentylhydroxylamine (14.1 g, 0.1398 mol) were mixed into toluene (200 mL) with p-toluenesulfonic acid monohydrate (1.0 g, 5.26 mmol). The mixture was refluxed for 3 hrs under argon atmosphere with a Dean-Stark trap to remove generated water. The solution was rotary evaporated to give a residue which was purified by flash chromatography over silica gel with EtOAc as an eluant and then recrystallization from a mixed solvent of hexanes and EtOAc. The title compound was obtained as a solid (21.24 g 65.1% yield), m.p. 95.1° C. (Rf =0.18 on a silica gel plate using hexanes:EtOAc, 2:1, v/v, as an eluant).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06046232
出典データセットuspto-grants-2000_04
ORD IDord-5830c77cdd0f46e8ad499356dc36ed7e
出典メモuspto-grants-2000_04