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Sodium Iodide → 3-Bromo-6-iodo-2-methylpyridine

HRID 1047291
ノート
印刷プレビュー

反応式

HRID 1047291 の反応式
[I-].[Na+].[Br:3][C:4]1[C:5]([CH3:11])=[N:6][C:7](Br)=[CH:8][CH:9]=1.[I:12][Si](C)(C)C>C(#N)CC.C(OCC)(=O)C.O>[Br:3][C:4]1[C:5]([CH3:11])=[N:6][C:7]([I:12])=[CH:8][CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 5238Sodium IodideHCID 85247Trimethylsilyl iodideHCID 27629463,6-Dibromo-2-methylpyridine

生成物 1

HCID 533020233-Bromo-6-iodo-2-methylpyridine収率 95%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 7854Propionitrile溶媒
HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
95 °C

実験手順

Sodium iodide (2 equiv) and 3,6-dibromo-2-methylpyridine (1 equiv) were combined in propionitrile and the resulting slurry was stirred under nitrogen for 5 min. Iodotrimethylsilane (0.2 equiv) was added and the reaction was heated at 95° C., with stirring, under nitrogen for 24 h. The slurry was cooled to room temperature, diluted with a 1:1 mixture of ethyl acetate and water. The mixture was agitated for 15 min and the aqueous and organic phases were then separated. The organic layer was washed sequentially with equal volumes of saturated aqueous sodium bicarbonate solution, sodium thiosulfate (5% aqueous solution), and saturated aqueous sodium chloride solution. The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford the desired product in 95% yield, as an oil, which crystallized to an off-white solid. MS (ESI) m/z 297.8 [M]+, 299.8 [M+2]+.

後処理

  1. stirringwith stirring, under nitrogen for 24 h
  2. temperatureThe slurry was cooled to room temperature
  3. stirringThe mixture was agitated for 15 min
  4. customthe aqueous and organic phases were then separated
  5. washThe organic layer was washed sequentially with equal volumes of saturated aqueous sodium bicarbonate solution, sodium thiosulfate (5% aqueous solution), and saturated aqueous sodium chloride solution
  6. dry with materialThe organic phase was dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f07883df31cb4523aa1935aa0f88967b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569494B2

反応ノート

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