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HRID 77898作成日:2026年10月24日

Acetic Acid → 4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine

https://huagongshe.com/ja/reaction/77898

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NitromethaneHCID 6375—
反応物Ammonium AcetateHCID 517165—
反応物4-(4-Methyl-pyridin-2-yloxymethyl)-benzaldehydeHCID 59255467—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255134109.4%

反応条件

温度100 °C

反応手順

To an acetic acid (20.0 mL) solution of 4-(4-methyl-pyridin-2-yloxymethyl)-benzaldehyde (2.60 g, 11.5 mmol) described in Manufacturing Example 43-1-2 were added nitromethane (3.50 g, 57.3 mmol) and ammonium acetate (1.76 g, 22.9 mmol) at room temperature under nitrogen atmosphere, which was stirred for 4 hours at 100° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.40 g) as a crude product.

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-cc6dd927238f4dbab11b01f4a7bf78c3
出典メモuspto-grants-2014_09