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HRID 20012作成日:2026年10月25日

Chloromethyl Methyl Ether → 2-Bromo-5-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/20012

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物Sodium hydrideHCID 24758—
反応物Sodium BicarbonateHCID 516892—
反応物2-Bromo-5-hydroxypyridineHCID 2762865—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-5-(methoxymethoxy)pyridineHCID 57433666—

反応手順

To a solution of 6-bromopyridin-3-ol (25 g, 144 mmol) in DMF (300 mL) at 0° C. under N2 is added portionwise NaH (5.7 g, 144 mmol) over 5 min. The reaction was stirred 1 h, then chloro(methoxy)methane (12 g, 144 mmol) was added and the reaction stirred an additional 1 h at 0° C. Saturated sodium bicarbonate (500 mL) was added slowly and the suspension stirred 30 min and warmed to rt. The solution was extracted with EtOAc (3×400 mL), the combined organic layers washed with H2O (500 mL), saturated NaCl (500 mL), dried (Na2SO4), and concentrated in vacuo to give the title compound as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745484B2
出典データセットuspto-grants-2010_06
ORD IDord-8139b49a9c4945e694dea03a4c0b2ea9
出典メモuspto-grants-2010_06