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HRID 1753作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/1753

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, 20% 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US05726315
出典データセットuspto-grants-1998_03
ORD IDord-d167806c04b646d4b1c49664d0f6f7f3
出典メモuspto-grants-1998_03