Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])N.[OH:11]S(O)(=O)=O.N([O-])=O.[Na+]>O>[Cl:1][C:2]1[CH:3]=[C:4]([OH:11])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a 0° C. solution of 3-chloro-4-methoxy aniline (1.0 g; 6.4 mmol) in 1:1 H2O:conc. H2SO4 (100 mL) was added very slowly a solution of NaNO2 (0.5 g; 7.6 mmol) in H2O (10 mL). Thick yellow fumes were emitted, and the black solution was then heated to reflux for 30 min. The mixture was extracted with EtOAc (4×50 mL) and the combined extracts were concentrated in vacuo. The residue was chromatographed (SiO2; 4:1 hex:EtOAc) to obtain 3-chloro-4-methoxy phenol (300 mg; 30%) as a yellow oil.
Aufarbeitung
- customTo a 0° C.
- temperaturethe black solution was then heated
- temperatureto reflux for 30 min
- extractionThe mixture was extracted with EtOAc (4×50 mL)
- concentrationthe combined extracts were concentrated in vacuo
- customThe residue was chromatographed (SiO2; 4:1 hex:EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-e28654bbf10d4c98af4bbd8e07de6718
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07084162B2
Verknüpfte Notizen
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