Triisopropyl borate → Boronic acid, [3-ethoxy-4-(1-methylethoxy)phenyl]-

HRID 1438098노트

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HRID 1438098 반응식
[CH2:1]([O:3][C:4]1[CH:9]=[C:8](I)[CH:7]=[CH:6][C:5]=1[O:11][CH:12]([CH3:14])[CH3:13])[CH3:2].[Li]CCCC.[B:20](OC(C)C)([O:25]C(C)C)[O:21]C(C)C>C1COCC1>[CH2:1]([O:3][C:4]1[CH:9]=[C:8]([B:20]([OH:25])[OH:21])[CH:7]=[CH:6][C:5]=1[O:11][CH:12]([CH3:14])[CH3:13])[CH3:2]

참가 물질

5

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온도
-78 °C

실험 절차

To a solution of 2-ethoxy-4-iodo-1-isopropoxybenzene (2.39 g, 7.8 mmol) in THF (25 mL) at −78° C., n-BuLi (1.6 M in hexanes, 6.83 mL, 1.4 eq) was slowly added. The reaction mixture was stirred at −78° C. for 20 min, followed by addition of triisopropyl borate (4.95 mL, 21.5 mmol). The mixture was stirred at −78° C. for 3.0 h and then warmed up to rt over 1.0 h. It was quenched by addition of 5% citric acid (20 mL), followed by a solution of Na2S2O3. After extraction with EtOAc and drying over Na2SO4, the crude product was purified by chromatography to give 1A (1.2 g, 67% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 1.41 (d, J=6.15 Hz, 6H) 1.49 (t, J=7.03 Hz, 3H) 4.21 (q, J=7.03 Hz, 2H) 4.64 (m, 1H) 7.02 (d, J=8.35 Hz, 1H) 7.70 (s, 1H) 7.79 (m, 1H).

후처리

  1. stirringThe mixture was stirred at −78° C. for 3.0 h
  2. temperaturewarmed up to rt over 1.0 h
  3. customIt was quenched by addition of 5% citric acid (20 mL)
  4. extractionAfter extraction with EtOAc
  5. dry with materialdrying over Na2SO4
  6. customthe crude product was purified by chromatography

출처 및 근거

ORD 기록
ord-c2813d17f22b445ea99806a096f594ed
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07622585B2

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