2-Phenylpyridine → 2-(2-Bromophenyl)pyridine

HRID 550326Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 550326
[C:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:13]Br>C(Cl)(Cl)Cl.[Fe]>[Br:13][C:6]1[CH:5]=[CH:4][CH:3]=[CH:2][C:1]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

3 g (19.3 mmol) of 2-phenylpyridine and 40 mg (0.716 mmol) of an iron powder were mixed and stirred. 4.0 g (25 mmol) of bromine was dropped paying attention to heat generation while stirring and cooling the mixture to 0° C., and the mixture was heated up to 90° C. and stirred for 10 hours. After completion of the reaction, this reaction mixture was dissolved in chloroform, and washed with a 5% aqueous sodium thiosulfate solution. The chloroform solution was dried over sodium sulfate, then, concentrated, and the residue was purified by silica gel column chromatography, to obtain the intended 2-(bromophenyl)pyridine.

Aufarbeitung

  1. temperatureto heat generation
  2. stirringwhile stirring
  3. temperaturethe mixture was heated up to 90° C.
  4. stirringstirred for 10 hours
  5. customAfter completion of the reaction
  6. washwashed with a 5% aqueous sodium thiosulfate solution
  7. dry with materialThe chloroform solution was dried over sodium sulfate
  8. concentrationconcentrated
  9. customthe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-66625216ddc04b3990b0170475934285
Quelldatensatz
uspto-grants-2011_05
Patentnummer
US07947340B2

Notizen zur Reaktion

Wird geladen…