Thionyl Chloride → 2-(2-Chloroethoxy)-1,3-dimethoxybenzene
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[C:4]=1[O:5][CH:6](O)[CH3:7].S(Cl)([Cl:17])=O>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[C:4]=1[O:5][CH2:6][CH2:7][Cl:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 7.77 g of 2,6-dimethoxyphenoxyethanol in 30 ml of pyridine was cooled and 4.7 g of thionylchloride was added with stirring. After 20 minutes, stirring, the reaction mixture was heated on the steam bath for 2 hours. After cooling, the reaction mixture was evaporated in reduced pressure. The residue was extracted with CHCl3, purified with silicagel chromatography (eluent: EtOAc) 1.82 g of objective compound was obtained.
Aufarbeitung
- stirringstirring
- temperaturethe reaction mixture was heated on the steam bath for 2 hours
- temperatureAfter cooling
- customthe reaction mixture was evaporated in reduced pressure
- extractionThe residue was extracted with CHCl3
- custompurified with silicagel chromatography (eluent: EtOAc) 1.82 g of objective compound
- customwas obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-607a922964134f7aa0ee55f90dc64397
- Quelldatensatz
- uspto-grants-1988_10
- Patentnummer
- US04780462
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