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HRID 1691055作成日:2026年10月27日

Acetic Acid → 2-(3-(2-Nitro-ethyl)-phenoxymethyl)-pyridine

https://huagongshe.com/reaction/1691055

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Sodium borohydrideHCID 4311764—
反応物2-(3-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridineHCID 59255249—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-(3-(2-Nitro-ethyl)-phenoxymethyl)-pyridineHCID 5925516464.3%

反応手順

To an acetic acid (2.5 mL) and dimethyl sulfoxide (43 mL) solution of 2-(3-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridine (2.56 g, 10 mmol) described in Manufacturing Example 60-1-2 was added sodium borohydride (605 mg, 16 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1.5 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1-4:1-1:1) to obtain the title compound (1.66 g, 64%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153662B2
出典データセットuspto-grants-2012_04
ORD IDord-f7f3f3ca9b2b4fa7838ddbf81dfa525c
出典メモuspto-grants-2012_04