2-Phenylpyridine → 2-(2-Bromophenyl)pyridine
Reaktionsgleichung
[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]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
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
- stirringwith stirring
- temperaturewatching heat generation, and it
- temperaturewas raised to 90° C.
- stirringstirred for 10 hours
- customAfter the reaction
- customto produce a solution, which
- washwas washed with 5% sodium thiosulfate aqueous solution
- dry with materialThe chloroform solution was dried with sodium sulfate
- concentrationconcentrated
- 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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