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Bromine → 3-BROMO-4-(4-FLUOROPHENYL)-4-OXOBUTANOIC ACID

HRID 903432
ノート
印刷プレビュー

反応式

HRID 903432 の反応式
[F:1][C:2]1[CH:14]=[CH:13][C:5]([C:6]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[O:7])=[CH:4][CH:3]=1.[Br:15]Br>C(O)(=O)C>[Br:15][CH:8]([C:6](=[O:7])[C:5]1[CH:4]=[CH:3][C:2]([F:1])=[CH:14][CH:13]=1)[CH2:9][C:10]([OH:12])=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408BromineHCID 1013593-(4-Fluorobenzoyl)propionic acid

生成物 1

HCID 38961393-BROMO-4-(4-FLUOROPHENYL)-4-OXOBUTANOIC ACID

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

To a solution of 19.62 g. of 3-(p-fluorobenzoyl)propionic acid in 100 ml. of acetic acid, is added 16 g. of bromine. The mixture is stirred for 18 hours and then the solvent is removed. Ice and water are added to the residue and the mixture is filtered. The solid is washed with water and then dissolved in 80 ml. of acetone. The solution is diluted with 400 ml. of hexane and allowed to evaporate, at room temperature, to a volume of 125 ml. A 100 ml. portion of hexane is added and the mixture is filtered, giving 24.6 g. of the desired product as tan crystals, m.p. 131°-135° C.

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

後処理

  1. customthe solvent is removed
  2. additionIce and water are added to the residue
  3. filtrationthe mixture is filtered
  4. washThe solid is washed with water
  5. dissolutiondissolved in 80 ml
  6. additionThe solution is diluted with 400 ml
  7. customto evaporate, at room temperature, to a volume of 125 ml
  8. additionportion of hexane is added
  9. filtrationthe mixture is filtered
  10. customgiving 24.6 g

出典と根拠

ORDレコード
ord-027d8f2861574c6a9afa6eb8802a6d03
出典データセット
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04226775

反応ノート

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