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

HRID 328627
ノート
印刷プレビュー

反応式

HRID 328627 の反応式
[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]
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 180AcetoneHCID 7841Allyl bromideHCID 97324-FluorophenolHCID 11430Potassium Carbonate

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-647e4a60349f4ef8aa0150ae4f015196
出典データセット
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04017631

反応ノート

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