2-Chloro-5-nitroanisole → 2-Chloro-5-nitrophenol
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[O:11]C>CC(O)=O.Br>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[OH:11]Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
2-Chloro-5-nitroanisole (9.7 g, 49.1 mmol) in HOAc (78 mL) and 48% HBr (97 mL) was heated for 18 h at 140° C. The reaction was cooled to RT, diluted with ice water, and extracted with EtOAc once the ice had melted. The organic layer was brine-washed 4×, dried over Na2SO4, filtered, concentrated, and dried under vacuum to yield the title compound as yellow-light brown solid.
Aufarbeitung
- extractionextracted with EtOAc once the ice
- washwashed 4×
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-e3d54c8fde044c86b06acf0bb34ff5e7
- Quelldatensatz
- uspto-grants-2009_05
- Patentnummer
- US07531553B2
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