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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 911436Erstellt: 25. Oktober 2026

Triethylamine → (R)-Methanesulfonic acid 1-(6-methyl-pyridin-2-yl)-ethyl ester

https://huagongshe.com/reaction/911436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt(R)-1-(6-methylpyridin-2-yl)ethanolHCID 45079484—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-Methanesulfonic acid 1-(6-methyl-pyridin-2-yl)-ethyl esterHCID 57656393100%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of (R)-1-(6-methyl-pyridin-2-yl)-ethanol (175 mg, 1.28 mmol) and triethylamine (355 μl, 2.56 mmol) in DCM (5 mL) at 0° C. add methanesulfonyl chloride (148 μl, 1.92 mmol). Stir at 0° C. for 30 min and quench the reaction mixture with saturated aqueous NaHCO3 at the same temperature. Extract the mixture three times with EtOAc, dry over anhydrous Na2SO4, and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (8:2) to give the title compound as a colorless oil (274 mg, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08022062B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-6032a6bb22f94cbebbbcac7c892c9f96
Quellennotizuspto-grants-2011_09