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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357762생성일: 2026년 10월 25일

Methyl 4-methylthiophene-2-carboxylate → 4-Methylthiophene-2-carboxylic acid

https://huagongshe.com/reaction/357762

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-methylthiophene-2-carboxylateHCID 2777593—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물4-Methylthiophene-2-carboxylic acidHCID 279458489.7%

반응 단계

5-Bromo-4-methyl-2-thiophenecarboxylic acid (3.33 g) was dissolved in dimethylformamide (50 ml), and potassium carbonate (4.0 g) and iodomethane (4.0 ml) were added. The mixture was stirred at room temperature for 2 hours, diluted with ethyl acetate, washed with 1N hydrochloric acid, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 5-bromo-4-methyl-2-thiophenecarboxylic acid methyl ester (3.47 g). A mixture of 5-bromo-4-methyl-2-thiophenecarboxylic acid methyl ester (2.36 g), zinc powder (1.65 g), acetic acid (10 ml) and water (10 ml) was stirred under reflux for 3 hours. Zinc powder (1 g) and acetic acid (10 ml) were further added. The mixture was stirred under reflux for 1 day, cooled, poured into concentrated aqueous ammonia and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4-methyl-2-thiophenecarboxylic acid methyl ester (1.42 g). 4-Methyl-2-thiophenecarboxylic acid methyl ester (1.42 g) was dissolved in a mixture of methanol (10 ml) and tetrahydrofuran (30 ml), and 1N aqueous sodium hydroxide (15 ml) was added. The mixture was stirred at room temperature for 1 hour and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4-methyl-2-thiophenecarboxylic acid (1.16 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840917
출처 데이터셋uspto-grants-1998_11
ORD IDord-124531e2276e4896aa4224d686010e2e
출처 메모uspto-grants-1998_11