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Hydrogen Peroxide → HCID 11819636, 화합물

HRID 2379812
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HRID 2379812 반응식
OO.[C:3]([NH:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)(=[O:5])[CH3:4].S([O-])([O-])=[O:16].[Na+].[Na+]>C(O)(=O)C>[C:3]([NH:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N+:10]=1[O-:16])(=[O:5])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 238301N-(2-(Pyridin-2-yl)ethyl)acetamide

생성물 1

HCID 11819636HCID 11819636, 화합물수율 100%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

30 wt % Hydrogen peroxide (80.3 ml) was added dropwise to a solution of 2-(2-acetylaminoethyl)pyridine (64.5 g) in acetic acid (65 ml) at 70°-75° C. and the mixture was stirred at the same temperature for 8 hours. After the mixture was ice-cooled and the mixture was added to a mixture of sodium sulfite (56.9 g) in ice water (200 ml). The solvent was removed by concentration in vacuo and the residue was extracted with a tetrahydrofuran. The extract solution was dried over magnesium sulfate and evaporated to give 2-(2-acetylaminoethyl)pyridine N-oxide (70.82 g).

후처리

  1. temperaturecooled
  2. customThe solvent was removed by concentration in vacuo
  3. extractionthe residue was extracted with a tetrahydrofuran
  4. dry with materialThe extract solution was dried over magnesium sulfate
  5. customevaporated

출처 및 근거

ORD 기록
ord-3a8a8d90f61f458e87a098b820b84eba
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05364871

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