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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1037305Erstellt: 26. Oktober 2026

Methyl iodide → 2-Chloro-3-methoxypyridine

https://huagongshe.com/reaction/1037305

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt2-Chloro-3-pyridinolHCID 81136—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Chloro-3-methoxypyridineHCID 10425279%

Reaktionsschritte

To a stirred solution of 2-chloro-3-hydroxypyridine (25.4 g, 196 mmol) in dry DMF (250 mL), at 0° C., was added sodium methoxide (11.5 g, 213 mmol). After 5 min, the reaction mixture was allowed to warm to RT. After 1 hour, the mixture was cooled to 0° C. and iodomethane (24 mL, 386 mmol) was added. The reaction mixture was stirred at 0° C. for 5 minutes, before allowing to warm to RT. After 2 hours, the reaction mixture was concentrated under reduced pressure. The resultant residue was partitioned between diethyl ether and water. The aqueous phase was isolated and extracted twice with diethyl ether. The combined organic extracts were washed with water, brine, dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (22.2 g, 79%) as an orange solid. LCMS (Method A): RT=2.76 min, [M+H]+=144/146.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08546376B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-c08ab2ebc3404938a14ddafb0f6dc8c4
Quellennotizuspto-grants-2013_10