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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1467962Erstellt: 25. Oktober 2026

Triethylamine → (2-Chloropyridin-4-yl)methyl methanesulfonate

https://huagongshe.com/reaction/1467962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt(2-Chloropyridin-4-yl)methanolHCID 7062237—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2-Chloropyridin-4-yl)methyl methanesulfonateHCID 5343676468,4%

Reaktionsschritte

To a stirred solution of (2-chloropyridin-4-yl)methanol (0.500 g, 3.496 mmol) in dichloromethane (15 mL), triethylamine (0.424 g, 4.195 mmol) and methanesulfonylchloride (0.440 g, 3.846 mmol) were added at 0° C. and stirred at room temperature for 2-3 h. The reaction was quenched with water and extracted with dichloromethane. The organic layer was concentrated in vacuo to give (2-chloropyridin-4-yl)methyl methanesulfonate (0.530 g, 68%); MS: 221.9 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09000175B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-dbe6dcafa19e4fc0b55dd62ddede6b56
Quellennotizuspto-grants-2015_04