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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1990831생성일: 2026년 10월 25일

Iodoethane → 3-Amino-5-ethoxy-4-iodo-benzoic acid methyl ester

https://huagongshe.com/reaction/1990831

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium t-butoxideHCID 23676156—
반응물Methyl 3-amino-5-hydroxy-4-iodobenzoateHCID 68458438—
용매DimethylformamideHCID 6228—
생성물3-Amino-5-ethoxy-4-iodo-benzoic acid methyl esterHCID 6845957969.6%

반응 단계

To a solution of 3-amino-5-hydroxy-4-iodo-benzoic acid methyl ester (0.25 g, 0.85 mmol, 1.0 equiv) in DMF (3 mL) and ethyl iodide (0.10 mL, 0.146 g, 0.94 mmol, 1.1 equiv) at 0° C. was added sodium tert-butoxide (0.11 g, 0.94 mmol, 1.1 equiv) in small portions over a time period of 10 min. After stirring for 1 h, the cooling bath was removed and the the reaction mixture stirred at rt for an additional 18 h. The solution was concentrated by evaporation under reduced pressure and extracted with ethyl acetate (3×50 mL). The combined organic phases were dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with hexane/ethyl acetate (2:1) yielding 0.19 g (69%) of the title compound. 1H NMR (250 MHz, CDCl3): δ 1.49 (t, J=7.0 Hz, 3H), 3.89 (s, 3H), 4.11 (q, J=7.0 Hz, 2H), 4.33 (br s, 2H), 6.82 (d, J=2.7 Hz, 1H), 7.07 (d, J=2.7 Hz, 1H). MS (EI): 321.0 [M]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07645753B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-0b0c52acce7342a5a4a7a0aa9ec4465f
출처 메모uspto-grants-2010_01