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HRID 4517作成日:2026年10月24日

Sodium hydride → Methyl 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoate

https://huagongshe.com/ja/reaction/4517

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Phosphorus pentachlorideHCID 24819—
反応物Methyl 3-HydroxybenzoateHCID 88068—
反応物1-Phenyl-1-(3-pyridyl)-2-propen-1-olHCID 12717096—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoateHCID 5407438396.5%

反応手順

Phosphorus pentachloride (3.0 g, 14.2 mmoles) was suspended in dichloromethane (4 ml). To the suspension was added dropwise a solution of 1-phenyl-1-(3-pyridyl)-2-propen-1-ol (2.0 g, 9.5 mmoles) in dichloromethane (20 ml) at 0° C., then the mixture was stirred for one hour at room temperature, followed by washing with water, saturated aqueous solution of sodium hydrogen carbonate in the order. The organic layer is dried (magnesium sulfate), and concentrated to about 20 ml at a temperature not exceeding 30° C. The solution was further dried with molecular sieves 4A. This solution was named as (a) solution. Separately, sodium hydride (400 mg, 10 mmoles) is suspended in dimethylformamide (5 ml). To the suspension was added dropwise methyl metahydroxybenzoate (1.37 g, 9.0 mmoles) dissolved in dimethylformamide (5 ml). The mixture was stirred for 30 minutes at 0° C., to which was added dropwise the (a) solution, followed by stirring at room temperature for 1.5 hours. The reaction mixture was poured in ice-water, which is subjected to extraction with ethyl acetate, washed with water and dried (magnesium sulfate), followed by removing the solvent by evaporation under reduced pressure. The residue was subjected to silica-gel column chromatography, using ether-ethyl acetate (7:3) as eluant to yield methyl 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoate (If-56) (3.0 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727078
出典データセットuspto-grants-1988_02
ORD IDord-5655146716e448659bad88b9b85685fd
出典メモuspto-grants-1988_02