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Chloroform → 3-(4-Methyl-5-(methylsulfonyl)-4H-1,2,4-triazol-3-yl)pyridine

HRID 732086
ノート
印刷プレビュー

反応式

HRID 732086 の反応式
[O-:1][Mn](=O)(=O)=O.[K+].[CH3:7][N:8]1[C:12]([S:13][CH3:14])=[N:11][N:10]=[C:9]1[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1.[OH-:21].[Na+].C(Cl)(Cl)Cl>O.C(O)(=O)C>[CH3:7][N:8]1[C:12]([S:13]([CH3:14])(=[O:1])=[O:21])=[N:11][N:10]=[C:9]1[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6212ChloroformHCID 14798Sodium HydroxideHCID 516875Potassium PermanganateHCID 404246263-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridine

生成物 1

HCID 469283343-(4-Methyl-5-(methylsulfonyl)-4H-1,2,4-triazol-3-yl)pyridine収率 53%

試薬・触媒・溶媒 2

HCID 176
Acetic Acid
溶媒
HCID 962Water溶媒

実験手順

KMnO4 (5 g, 32 mmol) was added to a solution of 3-[4-methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl]pyridine (6.0 g, 29 mmol) in H2O (40 mL) and acetic acid (100 mL). After 1 h stirring at rt the reaction was basified with aq. NaOH (4M). CHCl3 was added and the mixture was filtrated through celite. The layers were separated and the water phase was washed with CHCl3. The combined organic phase was dried and concentrated to give 3.67 g (53%) of the title compound. 1H NMR: 3.59 (s, 3H) 3.99 (s, 3H) 7.52 (m, 1H) 8.02 (dt, 1H) 8.83 (dd, 1H) 8.91 (m, 1H)

後処理

  1. filtrationthe mixture was filtrated through celite
  2. customThe layers were separated
  3. washthe water phase was washed with CHCl3
  4. customThe combined organic phase was dried
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-6294cd95bcec49d2a07551f1e036507c
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07585881B2

反応ノート

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