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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357768생성일: 2026년 10월 25일

Dimethylformamide → 2,5-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/357768

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물2,5-DimethylthiopheneHCID 12514—
반응물Phosphorus oxychlorideHCID 24813—
용매WaterHCID 962—
생성물2,5-Dimethylthiophene-3-carbaldehydeHCID 276275910.1%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840917
출처 데이터셋uspto-grants-1998_11
ORD IDord-5f2562df807c47ee9af68f2b2cff287a
출처 메모uspto-grants-1998_11