Reaktionsgleichung
O.[C:2]1([OH:10])[CH:9]=[C:7]([CH3:8])[CH:6]=[C:4]([OH:5])[CH:3]=1.[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[S:19](Cl)(=[O:21])=[O:20])#[N:12].C(OCC)C>C([O-])(O)=O.[Na+].O>[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[S:19]([O:5][C:4]1[CH:3]=[C:2]([OH:10])[CH:9]=[C:7]([CH3:8])[CH:6]=1)(=[O:21])=[O:20])#[N:12]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Orcinol monohydrate (1.42 g, 10.0 mmol) and 2-cyanobenzenesulfonyl chloride 2.02 g, 10.0 mmol) were mixed in saturated NaHCO3 (30 mL) and diethyl ether 30 mL). The biphasic mixture was stirred vigorously at room temperature overnight. The reaction mixture was diluted with water (50 mL) and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane to 5% ethyl acetate in dichloromethane) to give the title compound as a white solid (1.65 g, 57%). 1H-NMR (300 MHz, CDCl3) δ8.07 (m, 1H), 7.94 (m, 1H), 7.75-7.80 (m, 2H), 6.57 (s, 1H), 6.53 (s, 1H), 6.49 (s, 1H), 5,69 (br s, 1H), 2.22 (s, 3H).
Aufarbeitung
- extractionextracted into ethyl acetate (3×50 mL)
- washThe organic phase was washed with brine (2×50 mL)
- dry with materialdried over Na2SO4
- customAfter removing the solvent in vacuo
- customthe residue was purified by flash column chromatography (dichloromethane to 5% ethyl acetate in dichloromethane)
Quellen und Nachweise
- ORD-Eintrag
- ord-3903ca582462465b8aaa426a913ac73d
- Quelldatensatz
- uspto-grants-2001_05
- Patentnummer
- US06235778B1
Verknüpfte Notizen
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