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Potassium Carbonate → 2-Chloro-6-methyl-4-nitropyridine

HRID 333070
ノート
印刷プレビュー

反応式

HRID 333070 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH3:11])[N+:3]=1[O-].P(Cl)(Cl)Cl.C(=O)([O-])[O-].[K+].[K+]>C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH3:11])[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 24387Phosphorus trichlorideHCID 27518132-Chloro-6-methyl-4-nitropyridin-N-oxide

生成物 1

HCID 2986072-Chloro-6-methyl-4-nitropyridine

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

2-Chloro-4-nitro-6-methyl-pyridine 1-oxide (6.2 g, 0.033 mol) was dissolved in chloroform (100 ml), phosphorus trichloride was added (22.6 g, 0.165 mol) and the mixture was heated under reflux for 2 days. The mixture was cooled to room temperature, poured into icewater and the mixture was neutralized with solid potassium carbonate. The phases were separated, the aqueous phase was extracted three times with chloroform, the combined organic phases were dried over magnesium sulfate. The solvent was removed under reduced pressure after which 5.326 g of a brown oil was obtained (0.031 mol, 94%) which was used directly in the next step.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 days
  3. additionpoured into icewater
  4. customThe phases were separated
  5. extractionthe aqueous phase was extracted three times with chloroform
  6. dry with materialthe combined organic phases were dried over magnesium sulfate
  7. customThe solvent was removed under reduced pressure after which 5.326 g of a brown oil
  8. customwas obtained (0.031 mol, 94%) which

出典と根拠

ORDレコード
ord-24932a00954f403ea0716094da62e798
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08877934B2

反応ノート

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