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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 518404Erstellt: 25. Oktober 2026

Potassium Carbonate → 6-(Methylsulfonyl)pyridin-3-ol

https://huagongshe.com/reaction/518404

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktL-ProlineHCID 145742—
Edukt2-Chloro-5-hydroxypyridineHCID 819821—
EduktHCID 178504973HCID 178504973—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt6-(Methylsulfonyl)pyridin-3-olHCID 2314519644,9%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of 6-chloropyridin-3-ol (2.00 g, 15.44 mmol), MeSO2Na (2.36 g, 23.16 mmol), CuI (882.16 mg, 4.63 mmol), L-proline (533.28 mg, 4.63 mmol), and K2CO3 (640.19 mg, 4.63 mmol) in DMSO (20 mL) were charged into a microwave tube. The sealed tube was heated at 140° C. for 3 hrs under microwave. After cooling to room temperature, water (100 mL) was added. The mixture was extracted with EtOAc (100 mL×3). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography to give the title compound (1.2 g, 44.8%) as a yellow solid. 1H NMR (Methanol-d4, 400 MHz) δ 8.24 (d, J=2.4 Hz, 1H), 7.94 (d, J=8.4 Hz, 1H), 7.37 (dd, J1=8.8 Hz, J2=2.8 Hz, 1H), 3.15 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115114B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-11b931590f4240538a587e6d7b16418c
Quellennotizuspto-grants-2015_08