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Benzyl Alcohol → 4-(Benzyloxy)pyridine

HRID 861379
ノート
印刷プレビュー

反応式

HRID 861379 の反応式
[H-].[Na+].[CH2:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl[C:12]1[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=1>CS(C)=O>[CH2:3]([O:10][C:12]1[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
参加物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 244Benzyl AlcoholHCID 122884-ChloropyridineHCID 24758Sodium hydride

生成物 1

HCID 123288284-(Benzyloxy)pyridine収率 95%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

To a suspension of sodium hydride (80% dispersed in oil, 876 mg, 29.2 mmol) in DMSO (10 ml) was added benzyl alcohol (3 ml, 29.2 mmol) and the mixture stirred at room temperature for 1 hour. To this was added 4-chloropyridine (3.3 g, 29.2 mmol) and the reaction stirred at room temperature overnight. The precipitated sodium chloride was removed by filtration and the filtrate diluted with water (100 ml) and extracted with ether (3×120 ml). The combined organic layers were dried (MgSO4) and evaporated in vacuo to yield the title compound as an oil (4.8 g, 95%); δH (CDCl3) 5.11 (2H, s, PhCH2O), 6.87 (2H, d, J 6.3 Hz, 3-H, 5-H), 7.29-7.42 (5H, m, Ph), and 8.42 (2H, d, J 6.3 Hz, 2-H, 6-H).

後処理

  1. stirringthe reaction stirred at room temperature overnight
  2. customThe precipitated sodium chloride was removed by filtration
  3. additionthe filtrate diluted with water (100 ml)
  4. extractionextracted with ether (3×120 ml)
  5. dry with materialThe combined organic layers were dried (MgSO4)
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-8e1e4b65ad164f7ea1a076a8835be972
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05714498

反応ノート

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