Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 65038Erstellt: 24. Oktober 2026

Water → 1-(4-Methoxyphenyl)-2-(pyridin-3-yl)ethanone

https://huagongshe.com/de/reaction/65038

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt3-MethylpyridineHCID 7970—
EduktTetrahydrofuranHCID 8028—
EduktHexaneHCID 8058—
EduktButyllithiumHCID 178418339—
LösungsmittelDiisopropylamineHCID 7912—
Produkt1-(4-Methoxyphenyl)-2-(pyridin-3-yl)ethanoneHCID 23835185%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In 300 ml of anhydrous tetrahydrofuran was dissolved 33.2 ml of diisopropylamine, and the solution was cooled to -78° C., to which was added dropwise, while stirring, 148 ml of hexane solution of n-butyl lithium (1.6 M). The mixture was stirred for further 10 minutes at the same temperature, followed by dropwise addition of 20 g of β-picoline. The temperature was then raised up to -10°-0° C. and the mixture was stirred for 20 minutes, to which was added dropwise 19.4 g of ethyl p-anisole dissolved in 40 ml of anhydrous tetrahydrofuran. Then, the mixture was stirred for one hour at room temperature, followed by addition of about 100 ml of water. The organic solvent was evaporated off, and the concentrated solution was subjected to extraction with ethyl acetate. The extract solution was washed with water and dried on magnesium sulfate, followed by crystalliation from a mixture of ethyl acetate-isopropylether to give 20.8 g (yield: 85%) of 1-(4-methoxyphenyl)-2-(3-pyridyl)-ethanone, m.p. 71°-72° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04612321
Quelldatensatzuspto-grants-1986_09
ORD IDord-1cd4ccb5bc3a45e2ab408c62b1b1f9ac
Quellennotizuspto-grants-1986_09