Triisopropyl borate → HCID 57582338, 화합물

HRID 1094822노트

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HRID 1094822 반응식
Br[C:2]1[CH:7]=[C:6]([O:8][CH2:9][CH3:10])[CH:5]=[CH:4][C:3]=1[O:11][C:12]([F:15])([F:14])[F:13].C([Li])CCC.C([O:24][B:25](OC(C)C)[O:26]C(C)C)(C)C>O1CCCC1>[CH2:9]([O:8][C:6]1[CH:5]=[CH:4][C:3]([O:11][C:12]([F:15])([F:14])[F:13])=[C:2]([B:25]([OH:26])[OH:24])[CH:7]=1)[CH3:10]

참가 물질

5

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온도
-70 °C

실험 절차

To a stirred solution of the 2-bromo-4-ethoxy-1-trifluoromethoxy-benzene (Preparation 85, 884 mg, 3.10 mmol) in anhydrous tetrahydrofuran (10 ml) was added n butyl lithium (2M solution in cyclohexanes, 2.33 ml, 4.65 mmol) while maintaining the temperature below −70° C. under an atmosphere of nitrogen. The solution was stirred at this temperature for 1 hour then tri-isopropylborate (875 mg, 4.65 mmol) was added, and the reaction maintained at −70° C. for a further 2 hours. The reaction mixture was then quenched by the addition of ammonium chloride (aqueous solution) (5 ml), followed by acidification with hydrochloric acid (2N aqueous solution) (10 ml). The layers were separated and the organic layer was dried over anhydrous MgSO4 (s), filtered and evaporated in vacuo to afford crude title compound as a white solid (552 mg, 71%). Material was taken on without further purification.

후처리

  1. temperaturewhile maintaining the temperature below −70° C. under an atmosphere of nitrogen
  2. customThe reaction mixture was then quenched by the addition of ammonium chloride (aqueous solution) (5 ml)
  3. customThe layers were separated
  4. dry with materialthe organic layer was dried over anhydrous MgSO4 (s)
  5. filtrationfiltered
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-36ab218ae1804c98ad7f16ed775884dc
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08134007B2

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