Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1267944Erstellt: 26. Oktober 2026

Ethylene Oxide → 3-Bromo-4-(3-hydroxypropyl)pyridine

https://huagongshe.com/reaction/1267944

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene OxideHCID 6354—
EduktDiisopropylamineHCID 7912—
EduktHexaneHCID 8058—
Edukt3-Bromo-4-methylpyridineHCID 817630—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Bromo-4-(3-hydroxypropyl)pyridineHCID 1179059578,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Diisopropylamine (7.1 g, 70 mmol) is dissolved in THF (100 ml), and thereto is added a solution of n-butyl lithium in hexane (35.7 ml, 60 mmol) at −70° C., and the mixture is stirred for 15 minutes. Then, to the mixture is added a solution of 3-bromo-4-methylpyridine (8.6 g, 50 mmol) in THF (30 ml). Ten minutes thereafter, to the mixture is added ethylene oxide (2.6 g, 60 mmol), and the mixture is warmed to 0° C. over a period of time for one hour. The reaction is quenched with a saturated brine (50 ml), and the mixture is extracted with ethyl acetate (150 ml×2). The organic layer is washed with a saturated brine (100 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give the title compound (8.5 g) as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06555557B1
Quelldatensatzuspto-grants-2003_04
ORD IDord-a37ca3bf72b740b3ab1cd94928758083
Quellennotizuspto-grants-2003_04