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HRID 77952作成日:2026年10月24日

Acetic Acid → 1-Benzyloxy-3-(2-nitro-ethyl)-benzene

https://huagongshe.com/ja/reaction/77952

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3-Benzyloxy-trans-beta-nitrostyreneHCID 5368282—
溶媒Dimethyl SulfoxideHCID 679—
生成物1-Benzyloxy-3-(2-nitro-ethyl)-benzeneHCID 5925520557%

反応手順

To an acetic acid (5.5 mL) and dimethyl sulfoxide (94 mL) solution of 1-benzyloxy-3-((E)-2-nitro-vinyl)-benzene (5.5 g, 21.5 mmol) described in Manufacturing Example 61-1-2 was added sodium borohydride (1.3 g, 34.4 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) to obtain the title compound (3.14 g, 57%).

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-4abd74a6804f4b39a7e59581c3defcf2
出典メモuspto-grants-2014_09