Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])N.[OH:10]S(O)(=O)=O.N([O-])=O.[Na+]>O>[Br:1][C:2]1[CH:3]=[C:4]([OH:10])[CH:6]=[CH:7][C:8]=1[CH3:9]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a 0° C. mixture of 3-bromo-4-methyl aniline (5 g; 27 mmol) and H2SO4 (5.5 mL of a 16 M solution) in H2O (7.5 mL) was added dropwise a solution of aqueous NaNO2 (1.93 g; 28 mmol in 7.5 mL H2O). The reaction was stirred at 0° C. for 30 min, then was heated at 50° C. for 2 h, then was cooled to RT and extracted with EtOAc (2×). The combined organic extracts were washed with H2O, dried (Na2SO4) and concentrated in vacuo to give 3-bromo-4-methyl phenol (1.72 g; 34%) as an oil. This phenol was converted to 3-bromo-4-methyl phenyl chloroformate (1.9 g; 82%) using the same procedure (phosgene/dimethylaniline/heat) as for 3-fluoro-4-methyl phenyl chloroformate above.
Aufarbeitung
- temperaturewas heated at 50° C. for 2 h
- temperaturewas cooled to RT
- extractionextracted with EtOAc (2×)
- washThe combined organic extracts were washed with H2O
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-03e350e0a3fc454085162cb70907dbec
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07084162B2
Verknüpfte Notizen
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