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HRID 640076作成日:2026年10月24日

Acetic Acid → 1-Benzyloxy-4-(2-nitro-ethyl)-benzene

https://huagongshe.com/ja/reaction/640076

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(E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzeneHCID 5702926—
溶媒WaterHCID 962—
生成物1-Benzyloxy-4-(2-nitro-ethyl)-benzeneHCID 2472103770.8%

反応手順

To a mixture of 1-benzyloxy-4-((E)-2-nitro-vinyl)-benzene (1.0 g, 3.9 mmol) described in Manufacturing Example 1-1-1, acetic acid (1 mL) and dimethyl sulfoxide (17 mL) was added sodium borohydride (250 mg, 6.3 mmol) at room temperature while cooling appropriately, and the reaction mixture was stirred for 40 minutes at room temperature. Water was added to the reaction mixture. The reaction mixture was partitioned into ethyl acetate and water. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:3) to obtain the title compound (710 mg, 70%).

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-fa700799987242de8e389e439e3458f5
出典メモuspto-grants-2010_04