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HRID 264786作成日:2026年10月26日

Triphenylphosphine → 3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic Acid

https://huagongshe.com/reaction/264786

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Potassium AcetateHCID 517044—
反応物Potassium acrylateHCID 4429391—
反応物2-Bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridineHCID 19692711—
触媒Palladium ChlorideHCID 24290—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic AcidHCID 54021897—

反応条件

温度120 °C

反応手順

To a solution of 2-bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridine (5.00 g, 11.8 mmol) in DMF (22.8 ml) and water (1.2 ml) were added potassium acetate (2.91 g, 29.7 mmol), tetra-n-butylammonium iodide (4.37 g, 11.8 mmol), triphenylphosphine (0,245 g, 0.94 mmol), palladium chloride (83 mg, 0.47 mmol) and potassium acrylate (3.91 g, 35.4 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 3.3 h. Some potassium acrylate remained undissolved. The mixture was cooled, solids filtered and washed with ethyl acetate (2×60 ml). The filtrate was washed with water (250 ml) and with 5% sodium chloride solution (2×125 ml). The organic layer was dried and evaporated. The pure product was obtained by flash column chromatography (silica, 2,0% ether in dichloromethane) (3.52 g, 72%). mp 112°114° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646286
出典データセットuspto-grants-1997_07
ORD IDord-ea78dff7ba164da1b7519d695e39162b
出典メモuspto-grants-1997_07