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Benzyl Alcohol → 4-(Benzyloxy)pyridine

HRID 861379
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HRID 861379 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 244Benzyl AlcoholHCID 122884-ChloropyridineHCID 24758Sodium hydride

생성물 1

HCID 123288284-(Benzyloxy)pyridine수율 95%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-8e1e4b65ad164f7ea1a076a8835be972
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05714498

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