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Sulfuric Acid → 2-Chloro-4'-ethyl-1,1'-biphenyl

HRID 1283630
ノート
印刷プレビュー

反応式

HRID 1283630 の反応式
C(C1C=CC(C2C=CC=CC=2F)=CC=1)#C.[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[C:23]1[CH:28]=[CH:27][C:26]([C:29](=O)[CH3:30])=[CH:25][CH:24]=1.S(=O)(=O)(O)O>C1C=CC=CC=1>[CH2:29]([C:26]1[CH:27]=[CH:28][C:23]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[Cl:16])=[CH:24][CH:25]=1)[CH3:30]
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 3

HCID 1118Sulfuric AcidHCID 42040FluretofeneHCID 6120001-(2′-Chloro[1,1′-biphenyl]-4-yl)ethanone

生成物 1

HCID 132706352-Chloro-4'-ethyl-1,1'-biphenyl収率 64.5%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

The procedure of Example 1 was repeated, except that the 1-ethynyl-4-(2-fluorophenyl)benzene was replaced with 23.1 g of 4'-(2-chlorophenyl)acetophenone, the amount of benzene was increased to 150 ml, the amount of catalyst was increased to 3 g, the amount of sulfuric acid was increased to 2 ml, and the reduction was allowed to proceed for 13 hours. Evaporation of the benzene left a residue which was vacuum distilled to give 14 g of 1-ethyl-4-(2-chlorophenyl)benzene, bp 110°-112°/0.4 mm. The following elemental analysis was obtained:

後処理

  1. temperaturethe amount of catalyst was increased to 3 g
  2. customEvaporation of the benzene
  3. waitleft a residue which
  4. distillationdistilled

出典と根拠

ORDレコード
ord-e4a000bf51a645968d9c18ab21be4161
出典データセット
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03975542

反応ノート

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