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

HRID 1993908
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HRID 1993908 반응식
[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]
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참가 물질

6

반응물 2

HCID 5373977Ethyl 4-chlorocinnamateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 10921830Ethyl 3-(4-chlorophenyl)propanoate

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 10421208Zinc bromide촉매HCID 8857Ethyl Acetate용매

실험 절차

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]+.).

후처리

  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

출처 및 근거

ORD 기록
ord-f1131b1862374857aa7bbd6cbf0bacb1
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07652055B2

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