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Acetone → 1-Fluoro-4-(prop-2-en-1-yloxy)benzene

HRID 328627
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HRID 328627 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH2:9](Br)[CH:10]=[CH2:11].C(=O)([O-])[O-].[K+].[K+].CC(C)=O>O>[CH2:11]([O:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=1)[CH:10]=[CH2:9]
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참가 물질

6

반응물 4

HCID 180AcetoneHCID 7841Allyl bromideHCID 97324-FluorophenolHCID 11430Potassium Carbonate

생성물 1

HCID 6373421-Fluoro-4-(prop-2-en-1-yloxy)benzene

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 336.3 parts of 4-fluorophenol, 417.5 parts of allyl bromide, 420 parts of potassium carbonate and 480 parts of acetone is stirred and refluxed for 8 hours. After cooling to room temperature, 2250 parts of water are added. The aqueous layer is separated and extracted twice with ether. The combined extracts are washed successively twice with sodium hydroxide solution 10% and twice with sodium chloride solution, dried over potassium carbonate, filtered and evaporated. The oily residue is distilled in vacuo, yielding 381.8 parts of 4-allyloxy-fluorobenzene; bp. 93° C at 23 mm. pressure; nD20 : 1.4950; d2020 : 1.070.

후처리

  1. temperaturerefluxed for 8 hours
  2. customThe aqueous layer is separated
  3. extractionextracted twice with ether
  4. washThe combined extracts are washed successively twice with sodium hydroxide solution 10% and twice with sodium chloride solution
  5. dry with materialdried over potassium carbonate
  6. filtrationfiltered
  7. customevaporated
  8. distillationThe oily residue is distilled in vacuo

출처 및 근거

ORD 기록
ord-647e4a60349f4ef8aa0150ae4f015196
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04017631

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