Phenol → Ethyl 5-phenoxypentanoate

HRID 1059485노트

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HRID 1059485 반응식
[I-].[K+].C(=O)([O-])[O-].[K+].[K+].[C:9]1([OH:15])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:16]([O:18][C:19](=[O:25])[CH2:20][CH2:21][CH2:22][CH2:23]Br)[CH3:17]>CC(C)=O>[CH2:16]([O:18][C:19](=[O:25])[CH2:20][CH2:21][CH2:22][CH2:23][O:15][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:17]

참가 물질

6

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온도
60 °C

실험 절차

Dehydrated acetone of 240 ml was put in a 3-necked round-bottom flask, potassium iodide (0.06 mol), potassium carbonate (0.11 mol), and phenol (0.07 mol) were added to stir sufficiently. In this solution, 5-bromo valeric acid ethyl ester (0.06 mol) was dropped in a nitrogen atmosphere and refluxed at 60±5° C. to react for 24 hours. After completion of the reaction, a reaction solution was exsiccated to condensation using an evaporator, and dissolved again in methylene chloride, and water was added to the solution to separate and an organic layer was dehydrated by using magnesium sulfate anhydride followed by exsiccation for condensation using the evaporator. Hot methanol was added to a dried matter (reactant) yielded to dissolve and cooled slowly to precipitate again, resulting in a yield of 5-phenoxy valeric acid ethyl ester (PxVA). At this point, the yield ratio of this ester to 5-bromo valeric acid ethyl ester was 72 mol %.

후처리

  1. customto react for 24 hours
  2. customAfter completion of the reaction
  3. customa reaction solution was exsiccated to condensation
  4. customan evaporator
  5. dissolutiondissolved again in methylene chloride
  6. additionwater was added to the solution
  7. customto separate
  8. customfollowed by exsiccation for condensation
  9. customthe evaporator
  10. additionHot methanol was added to a dried matter (reactant)
  11. customyielded
  12. dissolutionto dissolve
  13. temperaturecooled slowly
  14. customto precipitate again

출처 및 근거

ORD 기록
ord-9b936323000149a798aba61ed3eda898
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06521429B2

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