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2-Methoxyethanol → 5-Bromo-2-(2-methoxyethoxy)pyridine

HRID 2170032
ノート
印刷プレビュー

反応式

HRID 2170032 の反応式
[CH3:1][O:2][CH2:3][CH2:4][OH:5].CC(C)([O-])C.[K+].[Br:12][C:13]1[CH:14]=[CH:15][C:16](Cl)=[N:17][CH:18]=1>O1CCOCC1.[Cl-].[Na+].O>[Br:12][C:13]1[CH:14]=[CH:15][C:16]([O:5][CH2:4][CH2:3][O:2][CH3:1])=[N:17][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 80192-MethoxyethanolHCID 27344145-Bromo-2-chloropyridineHCID 23665647Potassium tert-butoxide

生成物 1

HCID 225027175-Bromo-2-(2-methoxyethoxy)pyridine収率 73%

試薬・触媒・溶媒 2

HCID 312751,4-Dioxane溶媒HCID 57417360Sodium chloride; water溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

2-Methoxyethanol (5.12 mL, 85.0 mmol) was dissolved in 1,4-dioxane (125 ml). Potassium tert-butoxide (7.00 g, 62.4 mmol) was added under N2. The mixture was stirred for 10 minutes. 5-Bromo-2-chloropyridine (10.0 g, 52.0 mmol) was added and the resulting mixture was refluxed for 2 hours. The mixture was poured into brine and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4 and evaporated to dryness. Purification by flash chromatography (silica, heptanes/EtOAc 4:1) gave the title compound as a colorless oil (8.74 g, 73%) sufficiently pure for the next step.

後処理

  1. temperaturethe resulting mixture was refluxed for 2 hours
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed with brine
  4. dry with materialdried over MgSO4
  5. customevaporated to dryness
  6. customPurification by flash chromatography (silica, heptanes/EtOAc 4:1)

出典と根拠

ORDレコード
ord-6c2d02e6e6eb48fe8b2c539479d715a1
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09050327B2

反応ノート

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