Sodium Iodide → 2-((2-Chloro-4-nitrophenoxy)methyl)pyridine

HRID 1292961

반응식

HRID 1292961 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].Cl.[Cl-].[I-].[Na+].[C:16](#[N:18])[CH3:17]>>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:11][CH2:17][C:16]1[CH:4]=[CH:3][CH:2]=[CH:7][N:18]=1

참가 물질

5

반응물 4

HCID 5238Sodium IodideHCID 6342AcetonitrileHCID 12074NitrofunginHCID 6410751Hydrogen chloride dimer

생성물 1

HCID 174694332-((2-Chloro-4-nitrophenoxy)methyl)pyridine수율 52%

반응 조건

온도
60 °C

실험 절차

2-chloro-4-nitro phenol 10 g (57.6 mmol, 1 eq), 2-pycolyl chloride hydrogen chloride 9.45 g (57.6 mmol, 1 eq) cesium carbonate 41.3 (126.8 mmol, 2.2 eq) and sodium iodide 8.64 g (57.6 mmol, 1 eq) were suspended in 200 mL acetonitrile. The reaction mixture was stirred at 60° C. for 5 h. The resulted suspension was filtered and washed with 400 mL water, yielding 2-(2-chloro-4-nitro-phenoxymethyl)-pyridine (8 g, 52%) as a red solid.

후처리

  1. filtrationThe resulted suspension was filtered
  2. washwashed with 400 mL water

출처 및 근거

ORD 기록
ord-5dc39435a1b14a1da62c148cd06bcb13
출처 데이터셋
uspto-grants-2007_07
특허 번호
US07238701B2

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