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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2229529생성일: 2026년 10월 26일

Ethyl bromoacetate → [2-(4-Bromo-2-fluoro-benzylcarbamoyl)-5-chloro-phenoxy]-acetic acid ethyl ester

https://huagongshe.com/reaction/2229529

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참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Potassium CarbonateHCID 11430—
반응물N-(4-bromo-2-fluoro-benzyl)-4-chloro-2-hydroxy-benzamideHCID 18468196—
용매AcetoneHCID 180—
생성물[2-(4-Bromo-2-fluoro-benzylcarbamoyl)-5-chloro-phenoxy]-acetic acid ethyl esterHCID 2209347894%

반응 조건

온도50 °C

반응 단계

A solution of N-(4-bromo-2-fluoro-benzyl)-4-chloro-2-hydroxy-benzamide (3.25 g, 9.06 mmol) in acetone (45 mL, 0.2 M) was treated with aq K2CO3 (2 M, 6.8 mL, 14 mmol) and ethyl bromoacetate (1.2 mL, 11 mmol). After being heated to 50° C. for 8 h, the solution was cooled to room temperature and concentrated under reduced pressure until most of the acetone was removed. The solution was acidified to pH 1-2 with 2 N HCl, diluted with ethyl acetate and washed with saturated aq NaCl. The organic layer was dried over Na2SO4, filtered and concentrated. Purification by MPLC (10-60% ethyl acetate in heptane, 23 mL/min, 70 min) gave [2-(4-bromo-2-fluoro-benzylcarbamoyl)-5-chloro-phenoxy]-acetic acid ethyl ester as a white crystalline solid (3.78 g, 94%): mp 126-127° C.; Rf 0.61 (50% ethyl acetate in heptane); 1H NMR (DMSO-d6, 300 MHz) δ 8.90 (t, J=6 Hz, 1H), 7.82 (d, J=8.4 Hz, 1H), 7.52-7.47 (m, 1H), 7.39-7.31 (m, 2H),. 7.28 (d, J=1.8 Hz, 1H), 7.14 (dd, J=8.4 Hz, J2=1.8 Hz, 1H), 5.00, (s, 2H), 4.49 (d, J=6 Hz, 2H), 4.16 (q, J=7.2 Hz, 2H), 1.18 (t, J=6.6 Hz, 3H). ESI-LC/MS ml/z calcd for C18H16BrClFNO4: 444.7; found 446.0 (M+1)+. Anal. calcd for C18H16BrClFNO4: C, 48.62; H, 3.63; N, 3.15; Cl, 15.95. Found C, 48.57; H, 3.63; N, 3.11; Cl, 16.00.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06420426B1
출처 데이터셋uspto-grants-2002_07
ORD IDord-9f25a2161dc64fd1ae6a19dae6d75cc6
출처 메모uspto-grants-2002_07