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3-Hydroxybenzyl alcohol → 3-(Pyridin-2-yloxy)benzaldehyde

HRID 1678582
ノート
印刷プレビュー

反応式

HRID 1678582 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][CH:14]=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>N1C=CC=CC=1>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
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

5

反応物 3

HCID 1023-Hydroxybenzyl alcoholHCID 79732-BromopyridineHCID 11430Potassium Carbonate

生成物 1

HCID 27353633-(Pyridin-2-yloxy)benzaldehyde収率 61%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
90 °C

実験手順

3-Hydroxybenzyl alcohol (1.0 g, 8.2 mmol) was dissolved in pyridine (20 mL). 2-Bromopyridine (1.6 g, 9.8 mmol) and potassium carbonate (2.3 g, 16.4 mmol) were added thereto, and then the mixture was stirred at 90° C. for 10 minutes. Copper oxide(II) (1.6 g, 20.5 mmol) was further added thereto, and the reaction mixture was heated under reflux for 2 days. The reaction solution was filtered, and concentrated under reduced pressure. To the residue was added water, and the 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=100:0 to 70:30) to give the title compound (1.0 mg, yield 61%).

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 2 days
  3. filtrationThe reaction solution was filtered
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added water
  6. extractionthe mixture was extracted with ethyl acetate
  7. customThe extract was dried
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30)

出典と根拠

ORDレコード
ord-6c30dd5c1b6f42d292cc86e16b1882fc
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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