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Water → 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine

HRID 588370
ノート
印刷プレビュー

反応式

HRID 588370 の反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.OO.NC(N)=[O:13].FC(F)(F)C(OC(=O)C(F)(F)F)=O.O>C(Cl)Cl>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 9845Trifluoroacetic anhydrideHCID 31294Carbamide PeroxideHCID 876032-Chloro-3-methylpyridine

生成物 1

HCID 134316222-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine収率 86%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a mixture of 2-chloro-3-methylpyridine (15 g, 118 mmol) and urea hydrogen peroxide (44.07 g, 468.5 mmol) in DCM (300 mL) was added trifluoroacetic anhydride (98.55 g, 469.2 mmol) dropwise at 0° C. The mixture was stirred at room temperature for 20 h. The mixture was then poured into water (150 mL), and the layers were separated. The organic layer was washed with saturated aqueous Na2S2O3 (20 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1) to afford the title compound (14.5 g, 86%) as a colorless solid.

後処理

  1. customthe layers were separated
  2. washThe organic layer was washed with saturated aqueous Na2S2O3 (20 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1)

出典と根拠

ORDレコード
ord-9b19f3851e914078a67b2c5d960f976f
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227956B2

反応ノート

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