Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([CH2:13][CH3:14])=[C:10]([CH:15]3[C:19](=[O:20])[CH:18]=[CH:17][C:16]3=[O:21])[CH:9]=2)=[CH:4][CH:3]=1.[I-].[Mg+2].[I-].[O:25]1[CH:29]=[CH:28][CH:27]=[CH:26]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:12][C:11]([CH2:13][CH3:14])=[C:10]([CH:15]3[C:16](=[O:21])[CH:17]4[CH:18]([CH:26]5[O:25][CH:29]4[CH:28]=[CH:27]5)[C:19]3=[O:20])[CH:9]=2)=[CH:6][CH:7]=1Komponenten
4
Versuchsvorschrift
To a stirred solution of 2-[5-(4-chloro-phenyl)-2-ethyl-thiophen-3-yl]-cyclopent-4-ene-1,3-dione (248 mg, 0.78 mmol) in furan (3 ml) is added magnesium iodide (44 mg, 0.15 mmol) and the reaction allowed to stir at room temperature for 4 days. The crude reaction mixture is purified by flash chromatography to give 4-[5-(4-chloro-phenyl)-2-ethyl-thiophen-3-yl]-10-oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dione as a white solid (180 mg).
Aufarbeitung
- customThe crude reaction mixture
- customis purified by flash chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-b707357e38a34e0c99fef2ad9cc05794
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08530667B2
Verknüpfte Notizen
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