Reaktionsgleichung
C[O:2][C:3]1[CH:4]=[C:5]([S:9][C:10]2[CH:22]=[CH:21][C:13]3[O:14][C:15]([CH3:20])([CH3:19])[C:16]([CH3:18])=[CH:17][C:12]=3[CH:11]=2)[CH:6]=[CH:7][CH:8]=1.[I-].[Li+]>N1C(C)=CC(C)=CC=1C.ClCCl>[OH:2][C:3]1[CH:4]=[C:5]([S:9][C:10]2[CH:22]=[CH:21][C:13]3[O:14][C:15]([CH3:19])([CH3:20])[C:16]([CH3:18])=[CH:17][C:12]=3[CH:11]=2)[CH:6]=[CH:7][CH:8]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
6-(3-Methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (3.5 g) (see Preparation 6) was dissolved in dry 2,4,6-collidine (15 ml), anhydrous lithium iodide (3 g) was added and the mixture was heated under reflux under a nitrogen atmosphere for 24 hours. After cooling, the mixture was taken up in dichloromethane and washed with 2N aqueous hydrochloric acid solution (×3). The organic layer was dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the residue chromatographed on silica eluting with a solvent gradient of 1:1 hexane: dichloromethane changing to dichloromethane to yield 6-(3-hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (2.25 g) as an oil.
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux under a nitrogen atmosphere for 24 hours
- temperatureAfter cooling
- washwashed with 2N aqueous hydrochloric acid solution (×3)
- dry with materialThe organic layer was dried (anhydrous sodium sulphate)
- customthe solvent removed under reduced pressure
- customthe residue chromatographed on silica eluting with a solvent gradient of 1:1 hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-a410203f547f4664b9ec3d123e4e1b5a
- Quelldatensatz
- uspto-grants-1999_06
- Patentnummer
- US05912244
Verknüpfte Notizen
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