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Water → (4-Bromo-3-(trifluoromethoxy)phenyl)methanol

HRID 2235604
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HRID 2235604 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6](OC)=[O:7])=[CH:4][C:3]=1[O:12][C:13]([F:16])([F:15])[F:14].CC(C[AlH]CC(C)C)C.O>C1COCC1>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[O:12][C:13]([F:14])([F:16])[F:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14487Diisobutylaluminum hydrideHCID 59300634Methyl 4-bromo-3-(trifluoromethoxy)benzoate

생성물 1

HCID 54472733(4-Bromo-3-(trifluoromethoxy)phenyl)methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a cooled and stirred solution of methyl 4-bromo-3-(trifluoromethoxy)benzoate (28.2, 2.60 g, 8.70 mmol) in THF (20 mL) under nitrogen, was added DIBAL-H (19.2 mL, 1.0 M in toluene) at −78° C. The reaction mixture was stirred at 0° C. for 10 minutes and 5.0 mL of water was added. The resulting mixture was stirred at room temperature for 2 hours. The solid was then filtered off. EtOAc (100 mL) was added, and the mixture was washed with brine (20 mL) and dried with Na2SO4. The solvent was removed to give 28.3. 1H NMR (CDCl3) δ 1.91 (s, 1H), 4.71 (s, 2H), 7.18 (d, J=6.3 Hz, 1H), 7.36 (s, 1H), 7.63 (d, J=6.3 Hz, 1H).

후처리

  1. temperatureTo a cooled
  2. stirringThe resulting mixture was stirred at room temperature for 2 hours
  3. filtrationThe solid was then filtered off
  4. additionEtOAc (100 mL) was added
  5. washthe mixture was washed with brine (20 mL)
  6. dry with materialdried with Na2SO4
  7. customThe solvent was removed

출처 및 근거

ORD 기록
ord-30aa3966d7fd479dbe948beadfc36887
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714008B2

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