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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60806Erstellt: 24. Oktober 2026

Triethylamine → 2-(6-Methylpyridin-2-yl)ethyl methanesulfonate

https://huagongshe.com/de/reaction/60806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt6-Methylpyridine-2-ethanolHCID 70283—
LösungsmittelTolueneHCID 1140—
Produkt2-(6-Methylpyridin-2-yl)ethyl methanesulfonateHCID 87885158—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

MsCl (6.7 mmol, 0.52 mL) was added to a solution of 6-methyl-2-pyridineethanol (6.7 mmol, 0.92 g) and triethyl amine (13.4 mmol, 1.88 mL) in toluene (6 mL) at 0° C. dropwise. The resulting mixture was stirred at 0° C. for 30 min. The precipitate generated from reaction was filtered off. The filtrate was concentrated in vacuo to give crude 2-(6-methylpyridin-2-yl)ethyl methanesulfonate which was used for next step without further purification. A mixture of above described 2-(6-methylpyridin-2-yl)ethyl methanesulfonate, PhOH (13.4 mmol, 1.26 g) and NaOH (13.4 mmol, 0.54 g) in isopropanol (20 mL) was refluxed at 90° C. for 3 h. The reaction mixture was concentrated in vacuo and dissolved in EtOAc which was washed with water. The organic layer was separated, dried with MgSO4 and concentrated in vacuo. The crude product was purified by chromatography to give desired 2-methyl-6-(2-phenoxyethyl)pyridine as a colorless oil in 26% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440982B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-5815eb26c1a244d6995a88f54424a4fe
Quellennotizuspto-grants-2016_09