Ethyl Acetate → (2-Bromo-5-chloro-4-(4-ethylbenzyl)phenyl)methanol

HRID 1716957노트

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HRID 1716957 반응식
[Br:1][C:2]1[CH:11]=[C:10]([C:12](=O)[C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH3:20])=[CH:15][CH:14]=2)[C:9]([Cl:22])=[CH:8][C:3]=1[C:4](OC)=[O:5].C([SiH](CC)CC)C.FC(F)(F)S(O)(=O)=O.C(OCC)(=O)C>FC(F)(F)C(O)=O>[Br:1][C:2]1[CH:11]=[C:10]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH3:20])=[CH:15][CH:14]=2)[C:9]([Cl:22])=[CH:8][C:3]=1[CH2:4][OH:5]

참가 물질

6

실험 절차

To a solution of methyl 2-bromo-5-chloro-4-(4-ethylbenzoyl)benzoate (7.64 g, 20 mmol) in 2,2,2-trifluoroacetic acid (38 mL) was added to triethylsilane (5.88 mL, 40 mmol) under argon. After it was stirred for 10 min at room temperature, trifluoromethanesulfonic acid (0.1 mL) was added. The reaction temperature was raised from 26° C. to reflux. After stirring for 2 hours, TLC (petroleum ether:ethyl acetate=6:1, Rf=0.7) showed the reaction was complete. The reaction mixture was evaporated and the residue was dissolved in ethyl acetate (150 mL). The organic layer was washed 2× with H2O, 2× with NaHCO3, and 2× with brine, dried over anhydrous Na2SO4. Concentration under reduced pressure provided the title compound as a white solid. Yield: 7.2 g (100%). 1H NMR (CDCl3, 300 MHz) δ 7.85 (s, 1H), 7.44 (s, 1H), 7.17 (s, 1H), 7.14 (s, 1H), 7.10 (s, H), 7.07 (s, 1H), 4.05 (s, 2H), 3.92 (s, 3H), 2.63 (q, J=7.8 Hz, 2H), 1.24 (t, J=7.8 Hz, 3H).

후처리

  1. temperatureThe reaction temperature was raised from 26° C.
  2. temperatureto reflux
  3. stirringAfter stirring for 2 hours
  4. customThe reaction mixture was evaporated
  5. dissolutionthe residue was dissolved in ethyl acetate (150 mL)
  6. washThe organic layer was washed 2× with H2O, 2× with NaHCO3, and 2× with brine
  7. dry with materialdried over anhydrous Na2SO4
  8. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-3c2086a92527424eae4d2dc959589ca2
출처 데이터셋
uspto-grants-2010_09
특허 번호
US07803778B2

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