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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 718371생성일: 2026년 10월 24일

N-methyliminodiacetic acid → 2-(4-(4-Fluorophenethoxy)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione

https://huagongshe.com/ko/reaction/718371

반응식

참여 물질

역할이름HCID투입량
반응물N-methyliminodiacetic acidHCID 20441—
반응물(4-(4-Fluorophenethoxy)phenyl)boronic acidHCID 123643410—
용매Dimethyl SulfoxideHCID 679—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(4-(4-Fluorophenethoxy)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dioneHCID 13173416675.5%

반응 단계

A slurry of (4-(4-fluorophenethoxy)phenyl)boronic acid (122 g, 469 mmol) and 2,2′-(methylazanediyl)diacetic acid (76 g, 516 mmol) in anhydrous toluene (500 mL) and DMSO (200 mL) was refluxed for 4 h. Then, cooled, diluted with EtOAc (500 mL), washed with water (5×200 mL), brine (2×100 mL), dried (MgSO4), filtered and concentrated to give light orange foam which was purified by flash chromatography using 5-40% acetone/CH2Cl2 (5% increment per 2-lit) to afford 2-(4-(4-fluorophenethoxy)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (131.38 g, 354 mmol, 75% yield) as white solid. 1H NMR (500 MHz, CDCl3) δ 7.43 (d, J=8.4 Hz, 2H), 7.28-7.24 (m, 2H), 7.04-6.99 (m, 2H), 6.92 (d, J=8.5 Hz, 2H), 4.17 (t, J=6.9 Hz, 2H), 4.00 (d, J=16.6 Hz, 2H), 3.76 (d, J=16.6 Hz, 2H), 3.08 (t, J=6.8 Hz, 2H), 2.54 (s, 3H). LCMS (M+H)=372.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193720B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-08268ea527864686b0cb7d3da43ecca2
출처 메모uspto-grants-2015_11