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Water → 3-Iodo-6-methoxypyridazine

HRID 1378970
ノート
印刷プレビュー

反応式

HRID 1378970 の反応式
[I:1][C:2]1[N:3]=[N:4][C:5](I)=[CH:6][CH:7]=1.[CH3:9][O-:10].[Na+].O>CO>[CH3:9][O:10][C:5]1[N:4]=[N:3][C:2]([I:1])=[CH:7][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

5

反応物 3

HCID 962WaterHCID 2503833,6-DiiodopyridazineHCID 10942334Sodium Methoxide

生成物 1

HCID 2510323-Iodo-6-methoxypyridazine収率 86%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To 2.73 g (8.23 mmol) of 3,6-diiodopyridazine were added 80 ml of methanol and 3.17 g (16.46 mmol) of 28 wt % of sodium methylate in methanol, and the mixture was stirred at room temperature for 13 hours. Water was added to the reaction mixture, and the solution was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The obtained crude product was purified by silica-gel column chromatography (200 ml of silica gel, hexane:ethyl acetate=8:1) to give 1.661 g (7.04 mmol) of 3-methoxy-6-iodopyridazine (yield: 86%).

後処理

  1. extractionthe solution was extracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained crude product
  6. customwas purified by silica-gel column chromatography (200 ml of silica gel, hexane:ethyl acetate=8:1)

出典と根拠

ORDレコード
ord-f59764e9804d4fd486ac6fa0a785efe1
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05670492

反応ノート

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