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Ethylene Glycol → 3-(Pyridin-4-yloxy)propan-1-OL

HRID 1421015
ノート
印刷プレビュー

反応式

HRID 1421015 の反応式
Cl[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[CH2:8]([OH:11])[CH2:9]O.[OH-:12].[Na+].[CH3:14]S(C)=O>>[OH:12][CH2:14][CH2:9][CH2:8][O:11][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=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

5

反応物 4

HCID 174Ethylene GlycolHCID 679Dimethyl SulfoxideHCID 122884-ChloropyridineHCID 14798Sodium Hydroxide

生成物 1

HCID 219360073-(Pyridin-4-yloxy)propan-1-OL収率 45%

反応条件

温度
100 °C

実験手順

A mixture of 4-chloropyridine (7 g, 47 mmol), ethylene glycol (17.9 g, 235 mmol) and sodium hydroxide (4.67 g, 195 mmol) in DMSO (80 ml) was heated at 100° C. for 24 hours. Most of the solvent was removed by evaporation and the residue was diluted with ice water. The aqueous mixture was extracted with ethyl acetate, the extracts combined, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol mixtures (100/0 increasing to 97/3) to give 4-(3-hydroxypropoxy)pyridine (3.2 g, 45%).

後処理

  1. customMost of the solvent was removed by evaporation
  2. additionthe residue was diluted with ice water
  3. extractionThe aqueous mixture was extracted with ethyl acetate
  4. dry with materialdried (MgSO4)
  5. customthe solvent removed by evaporation
  6. customThe residue was purified by column chromatography
  7. washeluting with methylene chloride/methanol mixtures (100/0 increasing to 97/3)

出典と根拠

ORDレコード
ord-ce485901cf534c19a8dcbd1b815e3959
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06071921

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート