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

HRID 1674463Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1674463
[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-phenyl pyridine and 40 mg (0.716 mmol) of iron powder were mixed and stirred. It was cooled to 0° C. and 4.0 g (25 mmol) of bromine was added dropwise with stirring, and watching heat generation, and it was raised to 90° C., and stirred for 10 hours. After the reaction, this reaction mixture was dissolved in chloroform to produce a solution, which was washed with 5% sodium thiosulfate aqueous solution. The chloroform solution was dried with sodium sulfate, and then concentrated. The residue was purified by silica gel column chromatography, and the desired 2-(bromophenyl)pyridine was obtained.

Aufarbeitung

  1. stirringwith stirring
  2. temperaturewatching heat generation, and it
  3. temperaturewas raised to 90° C.
  4. stirringstirred for 10 hours
  5. customAfter the reaction
  6. customto produce a solution, which
  7. washwas washed with 5% sodium thiosulfate aqueous solution
  8. dry with materialThe chloroform solution was dried with sodium sulfate
  9. concentrationconcentrated
  10. customThe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-8958d83f4bb5430fae065f23e858a49b
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08003226B2

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