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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2303553Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2303553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-EthoxybenzaldehydeHCID 24834—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
EduktN-cyclopentylhydroxylamineHCID 10219393—
LösungsmittelTolueneHCID 1140—
Produktalpha-(4Ethoxyphenyl)-N-cyclopentylnitroneHCID 8658790865,1%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06433008B1
Quelldatensatzuspto-grants-2002_08
ORD IDord-dec44bf2cee347aeba511901d3e888aa
Quellennotizuspto-grants-2002_08