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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1158706Erstellt: 26. Oktober 2026

2-(Dimethylamino)ethanol → 2-Bromo-4-phenylpyridine

https://huagongshe.com/reaction/1158706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Dimethylamino)ethanolHCID 7902—
EduktCarbon tetrabromideHCID 11205—
Edukt4-PhenylpyridineHCID 13651—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
Produkt2-Bromo-4-phenylpyridineHCID 10470045,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2-dimethylaminoethanol (5.60 g, 62.8 mmol) in hexane (80 ml) was added dropwise 1.6N hexane solution of n-butyl lithium (78.5 ml, 125 mmol) under ice-cooling, and stirred at 0° C. for 30 minutes. Then, 4-phenylpyridine (3.24 g, 20.8 mmol) was added thereto, and stirred at 0° C. for 1 hour. After cooling the reaction solution to −78° C., a solution of carbon tetrabromide (25.0 g, 75.4 mmol) in hexane (40 ml) was added thereto, and stirred at −78° C. for 1 hour, then at room temperature for 1 hour. To the reaction solution was added water under ice-cooling, and extracted with ether. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduce pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the titled compound 2.21 g (45.4%) as solid product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812025B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-9d562519b434426ca73f9acfdde51242
Quellennotizuspto-grants-2010_10