Diisopropylamine → 1-Bromo-3-chloro-2,4-difluorobenzene

HRID 23164

Reaktionsgleichung

Reaktionsgleichung von HRID 23164
C(NC(C)C)(C)C.C([Li])CCC.[F:13][C:14]1[CH:19]=[C:18]([F:20])[CH:17]=[CH:16][C:15]=1[Br:21].[Cl:22]C(Cl)(Cl)C(C(Cl)(Cl)Cl)=O>O1CCCC1>[Cl:22][C:19]1[C:14]([F:13])=[C:15]([Br:21])[CH:16]=[CH:17][C:18]=1[F:20]

Komponenten

6

Edukt 4

HCID 7912DiisopropylamineHCID 8303HexachloroacetoneHCID 676741-Bromo-2,4-difluorobenzeneHCID 178418339Butyllithium

Produkt 1

HCID 27732561-Bromo-3-chloro-2,4-difluorobenzene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 19 ml (0.135 mole) of diisopropylamine in 125 ml of tetrahydrofuran (THF) cooled at −20° C. is added 80 ml of n-butyllithium (1.6 M in hexane). The temperature is raised to 0° C. for 5 minutes and lowered to −78° C. Then 25 g (0.129 mole) of 2,4-difluoro-bromobenzene is then added and the reaction is stirred at 65° C. for 2 hours. Then, 25 ml (0.164 mole) of hexachloroacetone is added and the solution is warmed at room temperature. After evaporation of the solvent, the residue is distilled under vacuum to give the desired product.

Aufarbeitung

  1. customlowered to −78° C
  2. temperaturethe solution is warmed at room temperature
  3. customAfter evaporation of the solvent
  4. distillationthe residue is distilled under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-26d3f179119941d39512cec2ecd01884
Quelldatensatz
uspto-grants-2005_02
Patentnummer
US06849740B2

Verknüpfte Notizen

Wird geladen…