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Hydrogen Peroxide → 2-Bromo-6-methylpyridine 1-oxide

HRID 37857
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인쇄 미리보기

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HRID 37857 반응식
[OH:1]O.[Br:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH3:10])[N:5]=1>C(O)(=O)C>[Br:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH3:10])[N+:5]=1[O-:1]
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 792052-Bromo-6-methylpyridine

생성물 1

HCID 36520842-Bromo-6-methylpyridine 1-oxide수율 75.2%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
90 °C

실험 절차

Hydrogen peroxide (30%, 1.76 mL, 17.4 mmol) was added to a solution of 2-bromo-6-methyl-pyridine (1.0 g, 5.80 mmol) in acetic acid (20 mL), and heated for 24 h at 90° C. The reaction mixture was cooled to ambient temperature, and partitioned between dichloromethane and water. The aqueous phase was separated and extracted with dichloromethane. The combined organic phases were washed thoroughly with water and dried over anhydrous sodium sulfate. Concentration in vacuo afforded 2-bromo-6-methyl-pyridine 1-oxide (820 mg, 75%) as a brown liquid which was used in the next step without further purification.

후처리

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. custompartitioned between dichloromethane and water
  3. customThe aqueous phase was separated
  4. extractionextracted with dichloromethane
  5. washThe combined organic phases were washed thoroughly with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationConcentration in vacuo

출처 및 근거

ORD 기록
ord-e7ec2c1329ad4d029fdc28cbdb7d8051
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524705B2

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