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HRID 78287作成日:2026年10月26日

Acetic Acid → 2-Benzyloxy-5-(2-nitro-ethyl)pyridine

https://huagongshe.com/reaction/78287

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WaterHCID 962—
反応物VertellusHCID 22959485—
反応物2-(Benzyloxy)-5-[(E)-2-nitroethenyl]pyridineHCID 56605146—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-Benzyloxy-5-(2-nitro-ethyl)pyridineHCID 5925506940.7%

反応手順

To a solution of 2-benzyloxy-5-((E)-2-nitro-vinyl)-pyridine described in Manufacturing Example 231-1-3 (44.0 g, 172 mmol) and acetic acid (44.0 mL) in dimethyl sulfoxide (200 mL) was added sodium borohydrate (11.0 g, 275 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes. Water was added to this reaction solution at room temperature while cooling appropriately, which was then partitioned into water and ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (18.1 g, 40.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-a18c599c3461453e87d6688ff1090134
出典メモuspto-grants-2014_09