Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li]C(C)(C)C.Br[C:14]1[CH:15]=[C:16]([CH:22]=[CH:23][CH:24]=1)[C:17](N(C)C)=[O:18].O>C1COCC1.CCCCC>[Br:1][C:2]1[CH:7]=[C:6]([C:17]([C:16]2[CH:22]=[CH:23][CH:24]=[CH:14][CH:15]=2)=[O:18])[CH:5]=[CH:4][CH:3]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -80 °C
Versuchsvorschrift
To a solution of 8.25 g (52.5 mmol) of bromobenzene in 100 mL of THF, 70 mL (105 mmol) of 2.5 M tBuLi in pentane was added dropwise with vigorous stirring for 2 h at −80° C. This mixture was slowly warmed to room temperature and then stirred for 30 min at this temperature. 11.4 g (50 mmol) of 3-bromo-N,N-dimethylbenzamide was added at 0° C., and the resulting mixture was stirred for 12 hr at room temperature. 150 mL of water was added, the organic solvent was evaporated using a rotary evaporator, and the product was extracted with 2×100 mL of dichloromethane. The combined extracts were dried over K2CO3 and then evaporated to dryness. This procedure gave 12.2 g (89%) of 16 which was further used without an additional purification.
Aufarbeitung
- temperatureThis mixture was slowly warmed to room temperature
- stirringstirred for 30 min at this temperature
- stirringthe resulting mixture was stirred for 12 hr at room temperature
- customthe organic solvent was evaporated
- customa rotary evaporator
- extractionthe product was extracted with 2×100 mL of dichloromethane
- dry with materialThe combined extracts were dried over K2CO3
- customevaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-bb629087c8004f54a980293da4baaddd
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08541522B2
Verknüpfte Notizen
Wird geladen…