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Hydrogen Peroxide → Pyridine, 3-cyclopropyl-, 1-oxide

HRID 2238668
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HRID 2238668 반응식
[CH:1]1([C:4]2[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=2)[CH2:3][CH2:2]1.[OH:10]O>C(O)(=O)C>[CH:1]1([C:4]2[CH:5]=[N+:6]([O-:10])[CH:7]=[CH:8][CH:9]=2)[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 120321433-cyclopropylpyridine

생성물 1

HCID 45079753Pyridine, 3-cyclopropyl-, 1-oxide수율 67.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

1.93 g of 3-cyclopropylpyridine (synthesized according to a method disclosed in Tetrahedron Lett. 2002, 39, 6987-6990) was dissolved in 15 mL of acetic acid, then 2.4 g of hydrogen peroxide solution (31%) was added thereto, and heated overnight under reflux. The reaction mixture was concentrated under reduced pressure, the obtained residue was dissolved in chloroform, and washed with a saturated aqueous solution of sodium hydrogen carbonate and water in the subsequent order. The organic layer was dried over anhydrous sodium sulfate. The insolubles were filtered, the filtrate was concentrated under reduced pressure, and 1.47 g of 3-cyclopropylpyridine 1-oxide [121-1] was obtained as a brown oily product.

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후처리

  1. temperatureheated overnight
  2. temperatureunder reflux
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. dissolutionthe obtained residue was dissolved in chloroform
  5. washwashed with a saturated aqueous solution of sodium hydrogen carbonate and water in the subsequent order
  6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  7. filtrationThe insolubles were filtered
  8. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-86cfe41842d04ccc9becbbdf8de00f38
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718801B2

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