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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535667Erstellt: 24. Oktober 2026

4-Toluenesulfonyl chloride → 2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/de/reaction/535667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
Edukt2-(6-Methoxypyridin-2-yl)ethan-1-olHCID 15319871—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonateHCID 59636776—

Reaktionsschritte

A solution of 2-(6-methoxypyridin-2-yl)ethanol (0.23 g, 1.50 mmol), 4-dimethylaminopyridine (0.028 g, 0.23 mmol), triethylamine (0.63 mL, 4.50 mmol) and p-toluenesulfonyl chloride (0.34 g, 1.80 mmol) in dry dichloromethane (5 mL) was stirred at rt over night. The solvent was removed in vacuo. Ethyl acetate and water were added. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried (Na2SO4) and concentrated. The product was purified by flash chromatography (SiO2; heptane/EtOAc, gradient 0-100%). Yield: 0.18 g (38%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859534B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-70334fdf56194307bd8210e70a762595
Quellennotizuspto-grants-2014_10