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Ethyl 4-chlorocinnamate → Ethyl 3-(4-chlorophenyl)propanoate

HRID 1993908
ノート
印刷プレビュー

反応式

HRID 1993908 の反応式
[CH2:1]([O:3][C:4](=[O:14])/[CH:5]=[CH:6]/[C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1)[CH3:2].[H][H]>C(OCC)(=O)C.[Pd].[Br-].[Zn+2].[Br-]>[CH2:1]([O:3][C:4](=[O:14])[CH2:5][CH2:6][C:7]1[CH:8]=[CH:9][C:10]([Cl:13])=[CH:11][CH:12]=1)[CH3:2]
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 2

HCID 5373977Ethyl 4-chlorocinnamateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 10921830Ethyl 3-(4-chlorophenyl)propanoate

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 10421208Zinc bromide触媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of (E)-3-(4-chloro-phenyl)-acrylic acid ethyl ester (0.37 g, 1.73 mmol) in ethyl acetate (10 ml) were added palladium on activated charcoal (18 mg) and zinc bromide (80 mg, 0.35 mmol). The reaction vessel was then pressurized with hydrogen gas to a pressure of 1 atmosphere and the mixture was stirred for 18 h. The catalyst was then removed by filtration, washing with ethyl acetate, and the filtrate was concentrated in vacuo to yield a colourless oil which was used for the next step without further purification; MS (ISP): 214.2, 212.1 ([M+H]+.).

後処理

  1. customThe catalyst was then removed by filtration
  2. washwashing with ethyl acetate
  3. concentrationthe filtrate was concentrated in vacuo
  4. customto yield a colourless oil which
  5. customwas used for the next step without further purification

出典と根拠

ORDレコード
ord-f1131b1862374857aa7bbd6cbf0bacb1
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07652055B2

反応ノート

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