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Hydrochloric Acid → 3-[4-(2-Fluorophenyl)benzoyl]propanoic acid

HRID 1491965
ノート
印刷プレビュー

反応式

HRID 1491965 の反応式
[Cl-].[Cl-].[Cl-].[Al+3].[C:5]1(=[O:11])[O:10][C:8](=[O:9])[CH2:7][CH2:6]1.[F:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.Cl>ClC(Cl)C>[F:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[C:19]1[CH:20]=[CH:21][C:22]([C:5]([CH2:6][CH2:7][C:8]([OH:10])=[O:9])=[O:11])=[CH:23][CH:24]=1
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 313Hydrochloric AcidHCID 7922Succinic anhydrideHCID 675792-FluorobiphenylHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 137582703-[4-(2-Fluorophenyl)benzoyl]propanoic acid収率 89%

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane溶媒

実験手順

To 6.2 g (46.5 mmol) of aluminum trichloride suspended in 50 ml of dichloroethane were added 3.02 g (30.2 retool) of succinic anhydride and 4.0 g (23.2 mmol) of 2-fluorobiphenyl were added thereto and the mixture was stirred at room temperature for 4 hours. The reaction solution was poured into hydrochloric acid containing ice, and extracted with chloroform. The organic layer was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and then recrystallized from chloroform to obtain 5.6 g (89% yield) of the desired compound.

後処理

  1. additionwere added
  2. additioncontaining ice
  3. extractionextracted with chloroform
  4. washThe organic layer was washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure
  7. customrecrystallized from chloroform

出典と根拠

ORDレコード
ord-0e962b3451d44d9785f54d4b747f2977
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05371225

反応ノート

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