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Methyl 4-[2-(4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate → Methyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoate

HRID 2187625
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HRID 2187625 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10]2[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][C:11]=2[C:20]([O:22][CH3:23])=[O:21])=[CH:4][CH:3]=1>[Pd].C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][C:10]2[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][C:11]=2[C:20]([O:22][CH3:23])=[O:21])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 53896095Methyl 4-[2-(4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate

생성물 1

HCID 18474597Methyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoate수율 96.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of methyl 4-[2-(4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate (56.75 g, 180.6 mmol), ethyl acetate (900 ml), 10% palladium on carbon (6 g) was stirred under an hydrogen atmosphere for 6 hours. The catalyst was filtered and replaced with fresh catalyst (6 g). The reaction was then stirred under an hydrogen atmosphere for 16 hours. The catalyst was filtered and the filtrate evaporated to dryness to give as a colourless gum, methyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoate (55.00 g).

후처리

  1. filtrationThe catalyst was filtered
  2. stirringThe reaction was then stirred under an hydrogen atmosphere for 16 hours
  3. filtrationThe catalyst was filtered
  4. customthe filtrate evaporated to dryness

출처 및 근거

ORD 기록
ord-0886a0e6aa554ea99215e0852e4f45a0
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410539B1

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