Dimethylformamide → 1H-Inden-1-one, 4-bromo-2,3-dihydro-5-(trifluoromethyl)-

HRID 1422610노트

반응식

HRID 1422610 반응식
C(Cl)(=O)C(Cl)=O.CN(C)C=O.[Br:12][C:13]1[C:18]([C:19]([F:22])([F:21])[F:20])=[CH:17][CH:16]=[CH:15][C:14]=1[CH2:23][CH2:24][C:25]([OH:27])=O>ClCCl>[Br:12][C:13]1[C:18]([C:19]([F:20])([F:21])[F:22])=[CH:17][CH:16]=[C:15]2[C:14]=1[CH2:23][CH2:24][C:25]2=[O:27]

참가 물질

5

실험 절차

Oxalyl chloride (6.8 mL) and N,N-dimethylformamide (0.1 mL) are added to a solution of 3-(2-bromo-3-trifluoromethyl-phenyl)-propionic acid (15.7 g) in dichloromethane (150 mL) at room temperature. The solution is stirred at reflux temperature for 2 h and then concentrated. Trifluoromethane-sulfonic acid (60 ml) is added to the residue, and the resulting mixture is stirred at 55° C. for 4 h. After cooling to room temperature, the mixture is poured into ice-cold water, and the resulting mixture is stirred for 5 min. The precipitate formed is separated by filtration, washed with water, and dissolved in ethyl acetate. The solution is washed with aqueous NaHCO3 solution, dried (Na2SO4), and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 90:10→80:20) to afford the title compound. LC (method 4): tR=1.04 min.

후처리

  1. temperatureat reflux temperature for 2 h
  2. concentrationconcentrated
  3. additionTrifluoromethane-sulfonic acid (60 ml) is added to the residue
  4. stirringthe resulting mixture is stirred at 55° C. for 4 h
  5. additionthe mixture is poured into ice-cold water
  6. stirringthe resulting mixture is stirred for 5 min
  7. customThe precipitate formed
  8. customis separated by filtration
  9. washwashed with water
  10. dissolutiondissolved in ethyl acetate
  11. washThe solution is washed with aqueous NaHCO3 solution
  12. dry with materialdried (Na2SO4)
  13. concentrationconcentrated
  14. customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 90:10→80:20)

출처 및 근거

ORD 기록
ord-3b50604e47994ae6a5cb55b647f07167
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08927531B2

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