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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(E)-4-(4-Fluoro-phenyl)-4-methyl-pent-2-enoic acid ethyl ester → 4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid ethyl ester

HRID 1026123
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반응식

HRID 1026123 반응식
[CH2:1]([O:3][C:4](=[O:17])/[CH:5]=[CH:6]/[C:7]([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)([CH3:9])[CH3:8])[CH3:2]>CO.[Pt](=O)=O>[CH2:1]([O:3][C:4](=[O:17])[CH2:5][CH2:6][C:7]([C:10]1[CH:11]=[CH:12][C:13]([F:16])=[CH:14][CH:15]=1)([CH3:9])[CH3:8])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67177264(E)-4-(4-Fluoro-phenyl)-4-methyl-pent-2-enoic acid ethyl ester

생성물 1

HCID 671771124-(4-Fluoro-phenyl)-4-methyl-pentanoic acid ethyl ester

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol용매

실험 절차

To a solution of (E)-4-(4-fluoro-phenyl)-4-methyl-pent-2-enoic acid ethyl ester (4.10 g) in methanol (150 ml) at room temperature was added platinum(IV) oxide (788 mg). The mixture was stirred under an atmosphere of hydrogen (1 atm) at room temperature for 2 h. The catalyst was removed by filtration and the filtrate was concentrated in vacuo to yield a yellow oil, (3.97 g, 96%); MS (ISP): 239.2 ([M+H]+).

후처리

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated in vacuo
  3. customto yield a yellow oil, (3.97 g, 96%)

출처 및 근거

ORD 기록
ord-4026d0ab01924658947eebdb4f517109
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729113B2

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