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2-Bromo-3-methylpyridine → 3-Methyl-2,2'-bipyridine

HRID 1970691
ノート
印刷プレビュー

反応式

HRID 1970691 の反応式
Br[C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1>O1CCCC1>[CH3:8][C:7]1[C:2]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=2)=[N:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 2208322-Bromo-3-methylpyridine

生成物 1

HCID 1824573-Methyl-2,2'-bipyridine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a flask were added 1.0 g 2-bromo-3-methylpyridine and 10 ml of dry tetrahydrofuran. The solution was purged with nitrogen and 34 mg tetrakis(triphenylphosphine)palladium was added followed by 17.4 ml of a 0.5M solution of 2-pyridylzinc bromide in tetrahydrofuran. The mixture was stirred at 22 C for 24 hours, then 40 C for 72 hours. The mixture was poured into a solution of 5 g EDTA, 2 g sodium carbonate and 40 ml water. The product was extracted twice with diethylether, washed with water and dried over sodium sulfate. Following filtration and solvent removal, the product was purified by silica gel chromatography using 48% ethyl acetate, 48% hexane and 4% methanol. A slightly yellow oil remained 0.38 g.

後処理

  1. customThe solution was purged with nitrogen and 34 mg tetrakis(triphenylphosphine)palladium
  2. additionwas added
  3. wait40 C for 72 hours
  4. additionThe mixture was poured into a solution of 5 g EDTA, 2 g sodium carbonate and 40 ml water
  5. extractionThe product was extracted twice with diethylether
  6. washwashed with water
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltration and solvent removal
  9. customthe product was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-a07a694b4402437fb59ea9384b26cf3e
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08431045B2

反応ノート

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