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HRID 640362作成日:2026年10月24日

Acetic Acid → 5-Fluoro-2-(3-fluoro-4-((E)-2-nitro-vinyl)phenoxymethyl)-pyridine

https://huagongshe.com/ja/reaction/640362

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2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehydeHCID 59255356—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-Fluoro-2-(3-fluoro-4-((E)-2-nitro-vinyl)phenoxymethyl)-pyridineHCID 5925507794.5%

反応条件

温度110 °C

反応手順

To an acetic acid (20.0 mL) solution of 2-fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)-benzaldehyde (901 mg, 3.62 mmol) described in Manufacturing Example 96-1-1 were added nitromethane (1.10 g, 18.1 mmol) and ammonium acetate (558 mg, 7.24 mmol) under nitrogen atmosphere, which was stirred for 2 hours at 110° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was 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 (1.00 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-704e668282074e309d700a70e2b2d372
出典メモuspto-grants-2010_04