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4-Fluorophenol → 4-Fluorophenyl 2-chlorobenzoate

HRID 128860
ノート
印刷プレビュー

反応式

HRID 128860 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[Cl:9][C:10]1[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=1[C:12](Cl)=[O:13]>N1C=CC=CC=1.C1(C)C=CC=CC=1>[Cl:9][C:10]1[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=1[C:12]([O:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=1)=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 97324-FluorophenolHCID 691102-Chlorobenzoyl chloride

生成物 1

HCID 27982194-Fluorophenyl 2-chlorobenzoate収率 87.8%

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 1140Toluene溶媒

実験手順

To a stirred solution of 25 g of 4fluorophenol in 40 cc of pyridine and 30 cc of toluene was added dropwise 40.9 g of 2-chlorobenzoylchloride at room temperature. And the resulting mixture was stirred at room temperature for 16 hours. Ice water was added to the reaction mixture and extracted with ethyl acetate. The ethylacetate layer was washed 4 times with 1N HCl , dried over magnesium sulfate. The solvent was distilled off and the crude product thus obtained was recrystallized from hexane to obtain 49.1 g of compound A. Yield: 87.8%.

後処理

  1. extractionextracted with ethyl acetate
  2. washThe ethylacetate layer was washed 4 times with 1N HCl
  3. dry with materialdried over magnesium sulfate
  4. distillationThe solvent was distilled off
  5. customthe crude product thus obtained
  6. customwas recrystallized from hexane

出典と根拠

ORDレコード
ord-d006fec14e8a4b3a9f079b861ca683a1
出典データセット
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05464863

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート