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HRID 640181作成日:2026年10月26日

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

https://huagongshe.com/reaction/640181

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US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-b0ce038c23fc4f83b436a88da5c852d5
出典メモuspto-grants-2010_04