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Potassium Iodide → 4-Allyloxybenzophenone

HRID 358381
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HRID 358381 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 4875Potassium IodideHCID 7850Allyl chlorideHCID 143474-HydroxybenzophenoneHCID 14797Potassium Hydroxide

생성물 1

HCID 2579104-Allyloxybenzophenone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-033a6afd5d024ad08e38130c84c05ddf
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04467082

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