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HRID 4521作成日:2026年10月24日

Dimethyl Sulfoxide → 7-Benzo[1,3]dioxol-5-yl-7-pyridin-3-yl-hept-6-enoic acid

https://huagongshe.com/ja/reaction/4521

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(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
反応物(2H-1,3-Benzodioxol-5-yl)(pyridin-3-yl)methanoneHCID 13285824—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物7-Benzo[1,3]dioxol-5-yl-7-pyridin-3-yl-hept-6-enoic acidHCID 1328583124.6%

反応条件

温度85 °C

反応手順

Sodium hydride (1 g, 60% in oil) was added to dimethyl sulfoxide (25 ml) under nitrogen and the mixture was heated at 85° C. with stirring for an hour. The reaction mixture was cooled to room temperature and 5-carboxypentyltriphenylphosphonium bromide (5.2 g, 11 mmoles) was added gradually. The mixture was stirred for 10 minutes and a solution of 3-(3,4-methylenedioxybenzoyl)pyridine (2.5 g, 0.11 mole) in tetrahydrofuran (10 ml) was added dropwise thereto. After completion of addition, the mixture was further stirred at room temperature for 30 minutes. After completion of the reaction, water (100 ml was added and the neutral substance was extracted twice with toluene (50 ml). The aqueous layer was adjusted to pH 5.5 with 2N hydrochloric acid and extracted with ethyl acetate. The organic 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 the eluent. The eluate was concentrated and the residue was crystallized from ethyl acetate-isopropyl ether to give (Z)-7-(3,4-methylenedioxyphenyl)-7-(3-pyridyl)-6-heptenoic acid (0.4 g, 24.6%). Mp 90°-91° 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-a74b6d8de3c74927ba4f80b2e8d86f3c
出典メモuspto-grants-1988_02