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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → HCID 20725604, 화합물

HRID 2190859
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HRID 2190859 반응식
[CH3:1][O:2][CH2:3][C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1.OO.C(=O)([O-])[O-:13].[Na+].[Na+]>C(O)(=O)C>[CH3:1][O:2][CH2:3][C:4]1[CH:5]=[N+:6]([O-:13])[CH:7]=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 784Hydrogen PeroxideHCID 10340Sodium CarbonateHCID 3389263-(Methoxymethyl)pyridine

생성물 1

HCID 20725604HCID 20725604, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
80 °C

실험 절차

A mixture of 7.74 g of 3-methoxymethylpyridine, 60 ml of acetic acid and 7.5 g of 30% hydrogen peroxide solution was stirred while heating at 80° C. for four hours. The reaction mixture was cooled to room temperature, and then sodium carbonate was added in small portions. The reaction mixture was subjected to filtration, and washed with ethyl acetate. The resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite and a saturated sodium chloride solution, and dried over anhydrous sodium carbonate. Activated carbon was added, followed by filtration through Celite™. The filtrate was concentrated under reduced pressure to give 2.66 g of 3-methoxymethylpyridine N-oxide.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationThe reaction mixture was subjected to filtration
  3. washwashed with ethyl acetate
  4. washThe resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite
  5. dry with materiala saturated sodium chloride solution, and dried over anhydrous sodium carbonate
  6. additionActivated carbon was added
  7. filtrationfollowed by filtration through Celite™
  8. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e58c21cc6e384f8a88263d6c280fd794
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324387B2

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