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3-Hydroxybenzyl alcohol → [3-(4-Fluorophenoxy)phenyl]methanol

HRID 1678580
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HRID 1678580 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].Br[C:11]1[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=1.C(=O)([O-])[O-].[K+].[K+].N1C2C(=CC=CC=2O)C=CC=1>CN1CCN(C)C1=O.O>[F:17][C:14]1[CH:15]=[CH:16][C:11]([O:1][C:2]2[CH:3]=[C:4]([CH2:5][OH:6])[CH:7]=[CH:8][CH:9]=2)=[CH:12][CH:13]=1
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참가 물질

7

반응물 4

HCID 1023-Hydroxybenzyl alcoholHCID 19238-HydroxyquinolineHCID 99931-Bromo-4-fluorobenzeneHCID 11430Potassium Carbonate

생성물 1

HCID 10584901[3-(4-Fluorophenoxy)phenyl]methanol수율 18%

시약·촉매·용매 2

HCID 962Water용매
HCID 6661
1,3-Dimethyl-2-imidazolidinone
용매

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온도
150 °C

실험 절차

3-Hydroxybenzyl alcohol (3.0 g, 24.6 mmol) was dissolved in 1,3-dimethyl-2-imidazolidinone (50 mL). 4-Bromofluorobenzene (6.5 g, 36.9 mmol), potassium carbonate (2.0 g, 14.8 mmol), 8-quinolinol (71 mg, 0.5 mmol), and copper chloride(I) (49 mg, 0.5 mmol) were added thereto, and then the mixture was stirred at 150° C. for 2 days. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=90:10 to 80:20) to give the title compound (0.98 mg, yield 18%).

후처리

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. customThe extract was dried
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified with silica gel column chromatography (hexane/ethyl acetate=90:10 to 80:20)

출처 및 근거

ORD 기록
ord-45e40532b07d4302beef479dedc63643
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008525B2

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