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HRID 640182作成日:2026年10月25日

Acetic Acid → 4-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridine

https://huagongshe.com/reaction/640182

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Dimethyl SulfoxideHCID 679—
反応物Sodium borohydrideHCID 4311764—
反応物4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255134—
溶媒WaterHCID 962—
生成物4-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridineHCID 5925521635.1%

反応手順

To a dimethyl sulfoxide (50 mL) solution of 4-methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (3.10 g, 11.5 mmol) described in Manufacturing Example 43-1-3 and acetic acid (3.10 mL) was added sodium borohydride (733 mg, 18.4 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes. Water was then added dropwise into the reaction solution at room temperature while cooling appropriately, and the reaction mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5→1:2) to obtain the title compound (1.10 g, 35.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-db22b7f433ae45f5a1f90af860b86697
出典メモuspto-grants-2010_04