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Z-4-(2-Fluoro-3-methoxyphenyl)-4-methylpent-2-enoic acid methyl ester → 4-(2-Fluoro-3-methoxyphenyl)-4-methylpentanoic acid methyl ester

HRID 1443149
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인쇄 미리보기

반응식

HRID 1443149 반응식
[CH3:1][O:2][C:3](=[O:18])/[CH:4]=[CH:5]\[C:6]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[C:10]=1[F:17])([CH3:8])[CH3:7]>C(O)C.[Pd]>[CH3:1][O:2][C:3](=[O:18])[CH2:4][CH2:5][C:6]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[C:10]=1[F:17])([CH3:8])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86599916Z-4-(2-Fluoro-3-methoxyphenyl)-4-methylpent-2-enoic acid methyl ester

생성물 1

HCID 179893004-(2-Fluoro-3-methoxyphenyl)-4-methylpentanoic acid methyl ester수율 83.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

23.30 g (84.33 mmol) of E/Z-4-(2-fluoro-3-methoxyphenyl)-4-methylpent-2-enoic acid methyl ester is mixed in 310 ml of ethanol with 1.2 g of palladium on carbon, and it is stirred under a hydrogen atmosphere overnight at room temperature. The catalyst is removed by filtration via a glass fiber filter, and the residue that remains after concentration by evaporation is chromatographed on silica gel (mobile solvent:ethyl acetate/hexane). 19.58 g (83.4%) of the desired compound is isolated.

후처리

  1. customThe catalyst is removed by filtration via a glass fiber
  2. filtrationfilter
  3. concentrationafter concentration
  4. customby evaporation
  5. customis chromatographed on silica gel (mobile solvent:ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-c2bfb8c7336445aaa23e76a9aabc468d
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07659297B2

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