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

HRID 1678580
ノート
印刷プレビュー

反応式

HRID 1678580 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6661
1,3-Dimethyl-2-imidazolidinone
溶媒

反応条件

温度
150 °C

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-45e40532b07d4302beef479dedc63643
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08008525B2

反応ノート

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