Isopropylhydroxylamine → alpha-(3,4-Ethylenedioxyphenyl)-N-isopropylnitrone
Reaktionsgleichung
[CH2:1]1[CH2:12][O:11][C:10]2[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=2[O:2]1.[CH:13]([NH:16][OH:17])([CH3:15])[CH3:14]>>[CH2:1]1[CH2:12][O:11][C:10]2[CH:9]=[CH:8][C:5]([CH:6]=[N+:16]([CH:13]([CH3:15])[CH3:14])[O-:17])=[CH:4][C:3]=2[O:2]1Komponenten
3
Versuchsvorschrift
The title compound was prepared according to the procedure described in Example 11 using 3,4-ethylenedioxybenzaldehyde and N-isopropylhydroxylamine. The crude produce was purified by column chromatography over silica gel using ethyl acetate as the eluant. The title compound was isolated in 53% yield as a solid, m.p. 108.8° C. (Rf=0.31 on a silica gel plate using EtOAc as the eluant).
Aufarbeitung
- customThe title compound was prepared
- customThe crude produce
- customwas purified by column chromatography over silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-42b02dc9ccfc4c72a6991830cfb7ac4d
- Quelldatensatz
- uspto-grants-2002_08
- Patentnummer
- US06441032B1
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