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HRID 4516作成日:2026年10月24日

Dimethyl Sulfoxide → (Z)-7-phenyl-7-pyridin-3-ylhept-6-enoic acid

https://huagongshe.com/ja/reaction/4516

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Phenyl-3-pyridinylmethanoneHCID 21540—
反応物Sodium hydrideHCID 24758—
反応物(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(Z)-7-phenyl-7-pyridin-3-ylhept-6-enoic acidHCID 653720180%

反応条件

温度80 °C

反応手順

To dimethylsulfoxide (40 ml) was added dropwise sodium hydride (1.0 g), and the mixture was heated at 80° C. for 30 minutes. The reaction mixture was cooled to room temperature, to which was added 5-carboxypentyltriphenyl phosphonium bromide (9.5 g, 21 mmoles) and the mixture was stirred for 5 minutes. To the reaction mixture was added a tetrahydrofuran solution (10 ml) of 3.7 g (0.02 mole) of 3-benzoylpyridine. The mixture was stirred for 30 minutes at room temperature, followed by addition of water (100 ml), which was subjected to extraction twice with ethylacetate (50 ml). The aqueous layers were combined and adjusted to pH 6 with 2N HCl, which was subjected to extraction with ethyl acetate. The organic layers were combined and washed with water and dried (magnesium sulfate). The solvent was then evaporated off, and the residue was subjected to silica-gel chromatography, using ethanolethyl acetate (1:5) as eluant to yield (E)+(Z)-7-(3-pyridyl)-7-phenyl-6-heptenoic acid (Ia-3, Ia-4 in Table 3) (4.5 g 79%).

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-4dcca75acd3843ae9e867d6f1684e2bb
出典メモuspto-grants-1988_02