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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357761생성일: 2026년 10월 26일

Ammonia → Methyl 4-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/357761

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물WaterHCID 962—
반응물Methyl 5-bromo-4-methylthiophene-2-carboxylateHCID 2795489—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
생성물Methyl 4-methylthiophene-2-carboxylateHCID 277759390.6%

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-e39cb44c2c214fe18cea3165f6428ddd
출처 메모uspto-grants-1998_11