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HRID 77806作成日:2026年10月26日

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

https://huagongshe.com/reaction/77806

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US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-8d3d40763f0c4de1a07f9332ef3d77f1
出典メモuspto-grants-2014_09