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Hydrogen Peroxide → 5-Fluoro-2-methylpyridine 1-oxide

HRID 1856
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HRID 1856 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[N:6][CH:7]=1.C(OO)(=[O:11])C.OO.C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C>[F:1][C:2]1[CH:7]=[N+:6]([O-:11])[C:5]([CH3:8])=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 784Hydrogen PeroxideHCID 6585Peracetic AcidHCID 11430Potassium CarbonateHCID 27628635-Fluoro-2-methylpyridine

생성물 1

HCID 196913065-Fluoro-2-methylpyridine 1-oxide수율 22%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
50 °C

실험 절차

To the solution of 5-fluoro-2-picoline obtained in Step 4, at 0° C., was added, with vigorous stirring, a cold solution of 40% peracetic acid (prepared by carefully adding 50 mL of 30% hydrogen peroxide solution to 150 mL of glacial acetic acid). The reaction mixture was heated at reflux temperature (50° C.) for 4 days and then poured into 600 mL of ice water. The aqueous mixture was adjusted to pH 9 by the addition of potassium carbonate and then was stirred at ambient temperature for 4 hours. The aqueous solution was continuously extracted with methylene chloride for 24 hours and the methylene chloride extract was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to afford 30.8 g (22% yield) of the title compound; MS DCI-NH3M/Z: 128 (M+H)+ base; 1H NMR (CDCl3) d 2.48 (s, 3H), 7.00 (ddd, 1H), 7.22 (dd, 1H), 8.22 (dd, 1H).

후처리

  1. temperatureThe reaction mixture was heated
  2. extractionThe aqueous solution was continuously extracted with methylene chloride for 24 hours
  3. extractionthe methylene chloride extract
  4. dry with materialwas dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c5f292609ba64fafa75e76f067d6b75e
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05726182

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