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HRID 357768作成日:2026年10月26日

Dimethylformamide → 2,5-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/357768

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2,5-DimethylthiopheneHCID 12514—
反応物Phosphorus oxychlorideHCID 24813—
溶媒WaterHCID 962—
生成物2,5-Dimethylthiophene-3-carbaldehydeHCID 276275910.1%

反応条件

温度100 °C

反応手順

Phosphorus oxychloride (10 ml) was slowly added dropwise to dimethylformamide (30 g) under ice-cooling, and 2,5-dimethylthiophene (11.2 g) was added. The mixture was stirred at 100° C. for 15 hours, poured into water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2,5-dimethyl-3-thiophenecarbaldehyde (1.41 g). 2,5-Dimethyl-3-thiophenecarbaldehyde (3.89 g) synthesized in this manner was dissolved in acetonitrile (30 ml), and sodium dihydrogen phosphate (1.2 g) in water (15 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added dropwise. The mixture was stirred at room temperature for 2 hours, alkalified with 1N aqueous sodium hydroxide and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 2,5-dimethyl-3-thiophenecarboxylic acid (4.09 g) as crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840917
出典データセットuspto-grants-1998_11
ORD IDord-5f2562df807c47ee9af68f2b2cff287a
出典メモuspto-grants-1998_11