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

HRID 452355Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 452355
[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-7a9e177fe2674b13aa753ee058bd7e03
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08492007B2

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