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HRID 1693906作成日:2026年10月25日

Nitromethane → 3-Benzyloxy-trans-beta-nitrostyrene

https://huagongshe.com/reaction/1693906

反応式

関与物質

役割名称HCID仕込み量
反応物NitromethaneHCID 6375—
反応物3-BenzyloxybenzaldehydeHCID 74342—
反応物Ammonium AcetateHCID 517165—
溶媒Acetic AcidHCID 176—
生成物3-Benzyloxy-trans-beta-nitrostyreneHCID 536828289%

反応条件

温度100 °C

反応手順

A mixture of 3-benzyloxy-benzaldehyde (5.16 g, 24.3 mmol) described in Manufacturing Example 61-1-1, nitromethane (2.16 mL, 48.6 mmol), ammonium acetate (2.81 g, 36.5 mmol) and acetic acid (50 mL) was stirred for 6 hours at 100° C. This mixture was cooled to room temperature, concentrated under a reduced pressure, and diluted with ethyl acetate. The organic layer was 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=4:1-2:1-1:1) to obtain the title compound (5.50 g, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08158657B2
出典データセットuspto-grants-2012_04
ORD IDord-abc7d048a59b42cea1bbe0df1b0e2579
出典メモuspto-grants-2012_04