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Iodine → 1,3,5-Trimethoxy-4-iodobenzene

HRID 919184
ノート
印刷プレビュー

反応式

HRID 919184 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[C:5]([O:11][CH3:12])[CH:4]=1.[I:13](O)(=O)=O.II>C(O)C>[I:13][C:4]1[C:5]([O:11][CH3:12])=[CH:6][C:7]([O:9][CH3:10])=[CH:8][C:3]=1[O:2][CH3:1]
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

5

反応物 3

HCID 807IodineHCID 24345Iodic acidHCID 693011,3,5-Trimethoxybenzene

生成物 1

HCID 122540971,3,5-Trimethoxy-4-iodobenzene収率 171.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

反応条件

温度
50 °C

実験手順

1,3,5-Trimethoxybenzene (14.5 g, 0.086 mol) was dissolved in 10 mL of ethanol at rt before warming to 50° C. in a waterbath after which, an aqueous solution of iodic acid (7.6 g, 0.043 mol) was added. Solid iodine (21.88 g, 0.086 mol) was dissolved in 20 mL of ethanol and the resultant solution was added portion-wise over 60 min to the reaction mixture. Stirring was continued at 50° C. until the color of I faded and a white precipitate appeared. The reaction mixture2 was stirred at room temperature for 18 h. The precipitate that formed was isolated via vacuum filtration, washed with ethanol and crystallized from methanol to yield 6 (21.7 g, 86%) as white crystals.

後処理

  1. customwas continued at 50° C. until the color of I
  2. stirringThe reaction mixture2 was stirred at room temperature for 18 h
  3. customThe precipitate that formed
  4. customwas isolated via vacuum filtration
  5. washwashed with ethanol
  6. customcrystallized from methanol

出典と根拠

ORDレコード
ord-b6e4dd6f4d394baebd2d549d931e414f
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09273021B2

反応ノート

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