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Water → 4'-Octyloxybiphenyl p-allyloxybenzoate

HRID 742523
ノート
印刷プレビュー

反応式

HRID 742523 の反応式
[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1)[CH:2]=[CH2:3].[CH2:14]([O:22][C:23]1[CH:28]=[CH:27][C:26]([C:29]2[CH:34]=[CH:33][C:32](O)=[CH:31][CH:30]=2)=[CH:25][CH:24]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21].O>C(Cl)(Cl)Cl>[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1)[CH:2]=[CH2:3].[CH2:14]([O:22][C:23]1[CH:24]=[CH:25][C:26]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:27][CH:28]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]
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 962WaterHCID 4606904-(Prop-2-en-1-yloxy)benzoic acidHCID 104943294-Hydroxy-4'-octyloxybiphenyl

生成物 1

HCID 867498084'-Octyloxybiphenyl p-allyloxybenzoate収率 86.2%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

15.0 g of PPE, 2.65 g (15.2 mmol) of the compound (12) and 4.50 g (13.4 mmol) of 4-octyloxy-4'-hydroxybiphenyl were dissolved in 120 ml of chloroform under an argon gas atmosphere and the whole was stirred at room temperature overnight. After addition of water to the reaction mixture, the whole was extracted with methylene chloride. After removal of the solvent by distillation, the residue was purified by silica gel column chromatography to obtain 5.30 g of 4- (4'-octyloxybiphenyl p-allyloxybenzoate (25) as a white solid (yield: 86.2%).

後処理

  1. extractionthe whole was extracted with methylene chloride
  2. customAfter removal of the solvent
  3. distillationby distillation
  4. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-8784e778b3304a33a343d1f6f676858a
出典データセット
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05554706

反応ノート

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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