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HRID 1690912作成日:2026年10月27日

Nitromethane → 2-Methyl-6-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine

https://huagongshe.com/reaction/1690912

反応式

関与物質

役割名称HCID仕込み量
反応物NitromethaneHCID 6375—
反応物Ammonium AcetateHCID 517165—
反応物4-(6-Methyl-pyridin-2-yloxymethyl)-benzaldehydeHCID 59255148—
溶媒Acetic AcidHCID 176—
生成物2-Methyl-6-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255368110%

反応条件

温度110 °C

反応手順

To a solution of 4-(6-methyl-pyridin-2-yloxymethyl)-benzaldehyde (4.19 g, 18.5 mmol) described in Manufacturing Example 3-1-2 in acetic acid (30 mL) were added nitromethane (5.65 g, 92.6 mmol) and ammonium acetate (2.85 g, 37.0 mmol) under nitrogen atmosphere, which was stirred for 3 hours at 110° C. The reaction mixture was partitioned into water and ethyl acetate. 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 to obtain the title compound (5.50 g) as a crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153662B2
出典データセットuspto-grants-2012_04
ORD IDord-086e68730a474775a518306be97f91e6
出典メモuspto-grants-2012_04