Reaktionsgleichung
[CH3:1][C:2]1[CH:8]=[C:7]([I:9])[C:6]([CH3:10])=[CH:5][C:3]=1[NH2:4].[C:11]([O:15][CH3:16])(=[O:14])[CH:12]=[CH2:13].[OH-].C([N+](C)(C)C)C1C=CC=CC=1.C1(C=CC(O)=CC=1)O>>[CH3:10][C:6]1[CH:5]=[C:3]([NH:4][CH2:13][CH2:12][C:11]([O:15][CH3:16])=[O:14])[C:2]([CH3:1])=[CH:8][C:7]=1[I:9]Komponenten
5
Versuchsvorschrift
15.0 g (0.061 mol) of 2,5-dimethyl-4-iodo-aniline, 55 ml of (0.611 mol) of methyl acrylate, 6 ml of benzyltrimethyl ammonium hydroxide and 0.3 g (3 mmol) of hydroquinone are refluxed for 11 days. Then the excess acrylate is distilled off and the residue is chromatographed on silica gel, eluting with methylene chloride.
Aufarbeitung
- distillationThen the excess acrylate is distilled off
- customthe residue is chromatographed on silica gel
- washeluting with methylene chloride
Quellen und Nachweise
- ORD-Eintrag
- ord-65e182c3e64e4a9287ee1088b3c7c16d
- Quelldatensatz
- uspto-grants-2002_11
- Patentnummer
- US06479524B1
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