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HRID 4522作成日:2026年10月24日

Dimethyl Sulfoxide → HCID 13285834、化合物

https://huagongshe.com/ja/reaction/4522

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Sodium hydrideHCID 24758—
反応物3-(2-Thenoyl)pyridineHCID 2760608—
反応物(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 13285834HCID 1328583429%

反応条件

温度85 °C

反応手順

Sodium hydride (60% in oil, 10 g, 0.25 mole) was added to dimethyl sulfoxide (250 ml) under argon and the mixture was stirred at 85° C. for an hour. The mixture was then cooled to room temperature and 5-carboxypentyltriphenylphosphonium bromide (52 g, 0.11 mole) was added gradually with the temperature being maintained at 40° C. The resulting mixture was stirred for 10 minutes, and a solution of 2-nicotinoylthiophene (20 g, 0.11 mole) in tetrahydrofuran (60 ml) was added dropwise. After the addition, the mixture was stirred at room temperature for 30 minutes, and water (300 ml) was added. The aqueous solution was extracted twice with toluene (300 ml) to remove the neutral substance. The aqueous layer was adjusted to pH 5.5 with 2N hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (magnesium sulfate) and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography using ethyl acetate as eluant and the eluate was concentrated. The resulting oily product was dissolved in ethyl acetate and the solution was allowed to stand overnight to give (Z)-7-(3-pyridyl)-7-(2-thienyl)-6-heptenoic acid (9 g, 29%). Mp 93°-94° C.

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-06b4a9fc73af486aaef1030ea95c72c8
出典メモuspto-grants-1988_02