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HRID 1037305作成日:2026年10月27日

Methyl iodide → 2-Chloro-3-methoxypyridine

https://huagongshe.com/reaction/1037305

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物2-Chloro-3-pyridinolHCID 81136—
反応物Sodium MethoxideHCID 10942334—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-3-methoxypyridineHCID 10425279%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546376B2
出典データセットuspto-grants-2013_10
ORD IDord-c08ab2ebc3404938a14ddafb0f6dc8c4
出典メモuspto-grants-2013_10