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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235083생성일: 2026년 10월 24일

Water → 5-Ethyl-2-thiophenecarboxylic acid, N-t-butyl amide

https://huagongshe.com/ko/reaction/235083

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Tert-ButylamineHCID 6385—
반응물Thionyl ChlorideHCID 24386—
반응물5-Ethylthiophene-2-carboxylic acidHCID 588192—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물5-Ethyl-2-thiophenecarboxylic acid, N-t-butyl amideHCID 6069932480%

반응 조건

온도0 °C

반응 단계

To a solution of 28 g (0.18 mol) of 5-ethyl-2-thiophenecarboxylic acid, from step 3a above, in 130 mL of methylene chloride was added a large excess (130 mL, 10 mol) of thionyl chloride, and the solution was heated at reflux for 2 hours. The solvent and excess reagent were removed by evaporation, and the residue was dissolved in 130 mL of chloroform and cooled to 0° C. To this solution was added 94 mL (0.9 mol) of t-butylamine dropwise, and the solution was stirred at reflux for 2 hours. The reaction was cooled, the solution poured into water, and the mixture extracted with ethyl acetate. The extract was washed with water and brine, dried, and concentrated. The residue was dissolved in ethyl acetate and the crude product was precipitated by addition of hexane. The crude product was collected by filtration and purified by flash chromatography over silica gel, eluting with 1:6 ethyl acetate:hexane, to afford 13.3 g (80% yield) of the title product after drying. MS 212 (M+H)+. NMR (CDCl3) δ: 7.25 (d, 1H, J=3 Hz), 6,72 (d, 1H, J=3 Hz), 5.70 (bs, 1H), 2.84 (q, 2H, J=7 Hz), 1.45 (s, 9H), 1.31 (t, 3H, J=7 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597832
출처 데이터셋uspto-grants-1997_01
ORD IDord-23b6fc38c21d44bf962b28e9020bf8fb
출처 메모uspto-grants-1997_01