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HRID 1284479作成日:2026年10月26日

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

https://huagongshe.com/reaction/1284479

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 mmole), 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 and the residue was subjected to a silica-gel chromatography using ethanol-ethyl acetate (1:5) as the eluent to yield (E)+(Z)-7-(3-pyridyl)-7-phenyl-6-heptenoic acid (A-3, I-4 in Table 10) (4.5 g 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04563446
出典データセットuspto-grants-1986_01
ORD IDord-5008650cf3cd4723bc36dc53b19561c3
出典メモuspto-grants-1986_01