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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl iodide → 3-(Methoxymethyl)pyridine

HRID 884981
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HRID 884981 반응식
[OH:1][CH2:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1.[CH2:9]1COCC1.[H-].[Na+].CI>O>[CH3:9][O:1][CH2:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1
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참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 75103-PyridinemethanolHCID 8028TetrahydrofuranHCID 24758Sodium hydride

생성물 1

HCID 3389263-(Methoxymethyl)pyridine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a mixture of 10.0 g of 3-hydroxymethylpyridine and 200 ml of THF, 3.7 g of 60% sodium hydride (in oil) was added in small portions at room temperature and then stirred for 15 minutes. To the reaction mixture, 13.0 g of methyl iodide was added dropwise, and the reaction mixture was stirred at room temperature for three hours. To the reaction mixture, 25 ml of water was added. Then, the reaction mixture was concentrated under reduced pressure. To the residue, 25 ml of water was added, followed by extraction with ethyl acetate three times. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 8.17 g of 3-methoxymethylpyridine.

후처리

  1. additionwas added in small portions at room temperature
  2. stirringthe reaction mixture was stirred at room temperature for three hours
  3. concentrationThen, the reaction mixture was concentrated under reduced pressure
  4. additionTo the residue, 25 ml of water was added
  5. extractionfollowed by extraction with ethyl acetate three times
  6. washThe combined organic layers were washed with a saturated sodium chloride solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-2d723532a4d44556b9c60bcc43d5b654
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242133B2

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