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Methyl iodide → 3-Bromo-2-methoxy-5-methylpyridine

HRID 554648
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HRID 554648 반응식
[Br:1][C:2]1[C:3]([OH:9])=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1.I[CH3:11]>C(Cl)(Cl)Cl.C(=O)([O-])[O-].[Ag+2]>[Br:1][C:2]1[C:3]([O:9][CH3:11])=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1
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참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 178430683HCID 178430683, 화합물

생성물 1

HCID 219527573-Bromo-2-methoxy-5-methylpyridine

시약·촉매·용매 2

HCID 178418647HCID 178418647, 화합물촉매HCID 6212Chloroform용매

반응 조건

온도
55 °C

실험 절차

3-Bromo-2-hydroxy-5-methylpyridine (5.012 g, 26.7 mmol), silver carbonate (9.58 g, 34.7 mmol), and iodomethane (5 mL, 80.0 mmol) were combined in CHCl3 (75 mL) and stirred at 55° C. for 3 hours. The mixture was cooled and filtered through Celite, and the filtrate was concentrated and purified by silica gel chromatography (0-100% EtOAc in hexanes) to give 3-bromo-2-methoxy-5-methyl-pyridine.

후처리

  1. temperatureThe mixture was cooled
  2. filtrationfiltered through Celite
  3. concentrationthe filtrate was concentrated
  4. custompurified by silica gel chromatography (0-100% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-3b4f135f3db4445382f3496dd8597d2c
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08049015B2

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