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Nitric Acid → 2-Chloro-5-methyl-4-nitropyridine N-oxide

HRID 271066
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HRID 271066 반응식
[N+:1]([O-:4])(O)=[O:2].[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([CH3:12])=[CH:8][N+:7]=1[O-:13].C(=O)([O-])[O-].[Na+].[Na+]>S(=O)(=O)(O)O>[Cl:5][C:6]1[CH:11]=[C:10]([N+:1]([O-:4])=[O:2])[C:9]([CH3:12])=[CH:8][N+:7]=1[O-:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 10340Sodium CarbonateHCID 134316232-Chloro-5-methylpyridin-1-ium-1-olate

생성물 1

HCID 123180102-Chloro-5-methyl-4-nitropyridine N-oxide수율 80%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

반응 조건

온도
100 °C

실험 절차

To a mixture of 165 mL of nitric acid and 209 mL of sulfuric acid was slowly added 56.4 g of 2-chloro-5-methylpyridine-1-oxide. The reaction mixture was stirred at 100° C. for two hours, cooled to room temperature, and added to ice. Sodium carbonate was added to adjust the pH to about pH 2 to pH 3. The resulting yellow solid was separated by filtration and washed with ice-water. The combined filtrates were extracted with hot chloroform. The extracts were combined, dried over sodium sulfate, and concentrated to give 59.1 g of 2-chloro-5-methyl-4-nitropyridine-1-oxide (80%). Mass Spec. M+H=189.

후처리

  1. temperaturecooled to room temperature
  2. additionadded to ice
  3. customThe resulting yellow solid was separated by filtration
  4. washwashed with ice-water
  5. extractionThe combined filtrates were extracted with hot chloroform
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-714a8f5a8b6f4df6a42c8845c85d676a
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452880B2

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