돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357769생성일: 2026년 10월 24일

Sodium Hydroxide → 2,5-Dimethylthiophene-3-carboxylic acid

https://huagongshe.com/ko/reaction/357769

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2,5-Dimethylthiophene-3-carbaldehydeHCID 2762759—
반응물Monosodium phosphateHCID 23672064—
용매Hydrogen PeroxideHCID 784—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물2,5-Dimethylthiophene-3-carboxylic acidHCID 819559261.8%

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-9f534f451f654a38b945d089223ed77d
출처 메모uspto-grants-1998_11