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HRID 13501作成日:2026年10月25日

p-Fluoronitrobenzene → Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylate

https://huagongshe.com/reaction/13501

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 5-hydroxypyridine-3-carboxylateHCID 354317—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
溶媒DimethylformamideHCID 6228—
生成物Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylateHCID 22040734—

反応条件

温度80 °C

反応手順

The mixture containing methyl-5-hydroxypyridine-3-carboxylate (1 eq), Potassium bis(trimethylsilyl)amide (1.2 eq) was stirred in N,N-dimethylformamide for 2 hours at room temperature. To this mixture was added 1-fluoro-4-nitrobenzene (1.1 eq) and Potassium carbonate (1.2 eq) and stirred at 80° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification on silica gel methyl-5-(4-nitrophenoxy)pyridine-3-carboxylate. MS: MH+=274.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-827bc1173d3441568cf390f6559fafd8
出典メモuspto-grants-2010_06