Phosphorus tribromide → 4-(Bromomethyl)-3,5-diethylpyridine
Reaktionsgleichung
[CH2:1]([C:3]1[CH:4]=[N:5][CH:6]=[C:7]([CH2:11][CH3:12])[C:8]=1[CH2:9]O)[CH3:2].[Br:13]P(Br)Br>C(Cl)(Cl)Cl>[Br:13][CH2:9][C:8]1[C:3]([CH2:1][CH3:2])=[CH:4][N:5]=[CH:6][C:7]=1[CH2:11][CH3:12]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of (3,5-diethylpyridin-4-yl)methanol (1.50 g, 9.07 mmol) in anhydrous chloroform (40 mL) at 0° C. was added dropwise tribromophosphane (2.48 g, 0.861 mL, 9.16 mmol). The reaction mixture was allowed to stir overnight at room temperature. The solvent was evaporated to provide crude 4-(bromomethyl)-3,5-diethylpyridine, which was used for the next step without any further purification; M+229.2.
Aufarbeitung
- customThe solvent was evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-364f30adfe7b498ab64830e3b4a6b168
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09315521B2
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