Nitric Acid → 2-Nitro-1-oxo-1lambda~5~-pyridine

HRID 1647084ノート

反応式

HRID 1647084 の反応式
OS(O)(=O)=O.C[C:7]1[C:12](C)=[CH:11][CH:10]=[CH:9][N+:8]=1[O-:14].C([O-])([O-])=O.[Na+].[Na+].[N+:21]([O-])([OH:23])=[O:22]>>[N+:21]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N+:8]=1[O-:14])([O-:23])=[O:22]

参加物

5

反応物 4

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 10340Sodium CarbonateHCID 3840573Pyridine, 2,3-dimethyl-, 1-oxide

生成物 1

HCID 124107812-Nitro-1-oxo-1lambda~5~-pyridine

実験手順

To 400 mL of concentrated H2SO4 was added slowly 130 g of impure 2,3-dimethylpyridine N-oxide. Fuming HNO3 (330 mL) was slowly added at a rate to keep the temperature between 120° C. and 170° C. After addition was complete, the temperature was held at 103° C. for 3 hours and then the reaction was cooled. The crude reaction was added to 1 kg ice in a large pan, then, with stirring, 1.1 kg Na2CO3 was added. After cooling to room temperature, the solids were removed by suction filtration from the solution. The filtrate was extracted with chloroform. The solids were washed with hot chloroform (3 times). The combined reduced organic extracts yielded 110 g of the crude desired nitropyridine N-oxide as an orange solid. ##STR8## 4-acetylamino-2,3-dimethylpyridine

後処理

  1. customthe temperature between 120° C. and 170° C
  2. additionAfter addition
  3. temperaturethe reaction was cooled
  4. customThe crude reaction
  5. customthe solids were removed by suction filtration from the solution
  6. extractionThe filtrate was extracted with chloroform
  7. washThe solids were washed with hot chloroform (3 times)

出典と根拠

ORDレコード
ord-2296f44a8546406794a00abe14060185
出典データセット
uspto-grants-1995_07
特許番号
US05430007

反応ノート

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