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Potassium Iodide → 4-Allyloxybenzophenone

HRID 358381
ノート
印刷プレビュー

反応式

HRID 358381 の反応式
[OH:1][C:2]1[CH:15]=[CH:14][C:5]([C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[OH-].[K+].[CH2:18](Cl)[CH:19]=[CH2:20].[I-].[K+]>O1CCCC1>[CH2:20]([O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:7])=[CH:14][CH:15]=1)[CH:19]=[CH2:18]
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 4875Potassium IodideHCID 7850Allyl chlorideHCID 143474-HydroxybenzophenoneHCID 14797Potassium Hydroxide

生成物 1

HCID 2579104-Allyloxybenzophenone

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

4-Hydroxybenzophenone (100 parts) was dissolved in tetrahydrofuran (100 parts). Potassium hydroxide (30.9 parts) was added, heated and stirred until completely dissolved. Allyl chloride (46.4 parts) and potassium iodide (42 parts) were added to this solution. The mixture was refluxed for 8 hours. After cooling, it was washed with water and the solvent removed by distillation. A crude product of the desired 4-allyloxybenzophenone was obtained. It was recrystallized in n-hexane to obtain 110 parts of 4-allyloxybenzophenone (melting point 71° C.) at 72% yield.

後処理

  1. temperatureheated
  2. dissolutionuntil completely dissolved
  3. temperatureThe mixture was refluxed for 8 hours
  4. temperatureAfter cooling
  5. washit was washed with water
  6. customthe solvent removed by distillation

出典と根拠

ORDレコード
ord-033a6afd5d024ad08e38130c84c05ddf
出典データセット
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04467082

反応ノート

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