Dimethylformamide → 3-Bromo-5-[1-(4-fluorophenyl)-1-hydroxyethyl]-benzaldehyde

HRID 53326노트

반응식

HRID 53326 반응식
C([Li])CCC.Br[C:7]1[CH:8]=[C:9]([C:14]([C:17]2[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=2)([CH3:16])[OH:15])[CH:10]=[C:11]([Br:13])[CH:12]=1.CN(C)[CH:26]=[O:27]>CCCCCC.C(OCC)C>[Br:13][C:11]1[CH:12]=[C:7]([CH:8]=[C:9]([C:14]([C:17]2[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=2)([OH:15])[CH3:16])[CH:10]=1)[CH:26]=[O:27]

참가 물질

6

실험 절차

A 2.5M solution of n-butyllithium in hexane (10.7 ml) was added dropwise to a stirred suspension of 3,5-dibromo-α-(4-fluorophenyl)-α-methylbenzenemethanol (5.90 g) in dry diethyl ether (160 ml) at -78° C. under an atmosphere of dry nitrogen. The resulting mixture was stirred at this temperature for 30 minutes and then N,N-dimethylformamide (2.93 g) was added dropwise. Stirring at -78° C. was continued for 1 hour and then the reaction was quenched by the addition of water. The temperature was allowed to reach room temperature and the organic layer was separated, washed with water and dried (MgSO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution was commenced with hexane/dichloromethane (1:1), and the ratio was gradually changed to hexane/dichloromethane (1:5). The later product fractions were combined and evaporated to give the title compound as an oil (2.10 g), Rf 0.15 (SS 1). Found: C,55.39; H,3.78. C15H12BrO2F requires C,55.75; H,3.74%.

후처리

  1. stirringStirring at -78° C.
  2. waitwas continued for 1 hour
  3. customthe reaction was quenched by the addition of water
  4. customto reach room temperature
  5. customthe organic layer was separated
  6. washwashed with water
  7. dry with materialdried (MgSO4)
  8. customEvaporation of the solvent
  9. customgave an oil which
  10. customwas chromatographed on silica gel
  11. washElution
  12. customevaporated

출처 및 근거

ORD 기록
ord-6a363400835b4485b1a03f181c05d368
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05618941

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