Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][C:3]([CH:6]=O)=[CH:2]1.[CH3:8][C:9]1([C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[C:13](=[O:14])[CH:12]=[C:11]([CH3:15])[O:10]1.[OH-].[Na+].[Cl-].[Na+]>C(O)C>[F:22][C:19]1[CH:20]=[CH:21][C:16]([C:9]2([CH3:8])[C:13](=[O:14])[CH:12]=[C:11]([CH:15]=[CH:6][C:3]3[CH:4]=[CH:5][S:1][CH:2]=3)[O:10]2)=[CH:17][CH:18]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-thiophenecarboxaldehyde (1.3 g, 1.2 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (75 mL), was added 1N aqueous sodium hydroxide (2 mL, 2 mM). The reaction solution was stirred at room temperature for one day. After saturated aqueous sodium chloride (400 mL) was added, the aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a brown oil. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford a yellow solid (1.8 g, 62% yield), m.p. 97°-98° C.
Aufarbeitung
- extractionthe aqueous layer was extracted with dichloromethane (3×100 mL)
- washThe combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto give a brown oil
- customThe crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-86b3919747e04f9683e021ce45808f74
- Quelldatensatz
- uspto-grants-1991_03
- Patentnummer
- US05001126
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