Dimethylformamide → 3-Bromo-5-fluorobenzaldehyde

HRID 20453

반응식

HRID 20453 반응식
Br[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([Br:9])[CH:3]=1.C([Li])CCC.CN(C)[CH:17]=[O:18]>O1CCCC1>[Br:9][C:4]1[CH:3]=[C:2]([CH:7]=[C:6]([F:8])[CH:5]=1)[CH:17]=[O:18]

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

Add dropwise a solution of 1,3-dibromo-5-fluorobenzene (12.39 mL, 98.5 mmol) in tetrahydrofuran (20 mL) to a solution of n-butyllithium (64.61 mL, 103.4 mmol, 1.6 M in hexanes) in tetrahydrofuran (55 mL) at −78° C. Stir at −78° C. for 45 minutes, add dimethylformamide (7.62 mL, 98.5 mmol), stir at −78° C. for 1.5 hours, remove cooling bath and stir 10 minutes. Add saturated aqueous ammonium chloride (150 mL) and extract with diethyl ether (2×700 mL). Wash combined organic layers sequentially with water (1×300 mL) and saturated aqueous sodium chloride (1×300 mL). Dry over magnesium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes to provide the desired compound (11.05 g, 55.3%).

후처리

  1. stirringstir at −78° C. for 1.5 hours
  2. customremove
  3. temperaturecooling bath
  4. stirringstir 10 minutes
  5. extractionAdd saturated aqueous ammonium chloride (150 mL) and extract with diethyl ether (2×700 mL)
  6. washWash
  7. dry with materialDry over magnesium sulfate
  8. concentrationconcentrate under reduced pressure
  9. washSubject residue to silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-b4e139e6572d4378a1be70b4ffd45f05
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745438B2

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