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HRID 55258作成日:2026年10月25日

Methyl Acrylate → (E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoate

https://huagongshe.com/reaction/55258

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl AcrylateHCID 7294—
反応物Potassium CarbonateHCID 11430—
反応物3-Benzyloxy-2-iodopyridineHCID 19957501—
触媒Tetrabutylammonium BromideHCID 74236—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物(E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoateHCID 22161738—

反応条件

温度100 °C

反応手順

5.2 g of palladium(II) acetate, 77.8 g of potassium carbonate and 72.5 g of tetrabutylammonium bromide are added to a solution of 70 g of 3-benzyloxy-2-iodopyridine and 39.8 ml of acrylic acid methyl ester in 120 ml of dimethylformamide, and the suspension is stirred under argon atmosphere for 10 hours at 100° C. (bath temperature). The reaction mixture is concentrated by evaporation in a vacuum, the residue is added to water and shaken out with ethyl acetate. The organic phase is washed three times with water and once with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation. The crude product is chromatographed on silica gel with hexane/10-25% ethyl acetate. 48.2 g of 3-(3-benzyloxy-2-pyridyl)-(2E)-2-propenoic acid methyl ester is obtained as oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624943
出典データセットuspto-grants-1997_04
ORD IDord-d4846378d04a4d3fb9385b65082d0c14
出典メモuspto-grants-1997_04