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3-(4-t-Butyloxycarbonylphenyl)acrylic acid ethyl ester → Tert-butyl 4-(3-ethoxy-3-oxopropyl)benzoate

HRID 1252231
노트
인쇄 미리보기

반응식

HRID 1252231 반응식
[CH2:1]([O:3][C:4](=[O:20])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[CH:9][CH:8]=1)[CH3:2]>C(O)C.[Pd]>[CH2:1]([O:3][C:4](=[O:20])[CH2:5][CH2:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[CH:11][CH:12]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 537912813-(4-t-Butyloxycarbonylphenyl)acrylic acid ethyl ester

생성물 1

HCID 9993703Tert-butyl 4-(3-ethoxy-3-oxopropyl)benzoate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 3-(4-t-butyloxycarbonylphenyl)acrylic acid ethyl ester (11.52 g) and 5% palladium-charcoal in ethanol (115 ml) was stirred under hydrogen atmosphere at room temperature. The catalyst was removed by filtration and washed with ethanol. The combined solution was evaporated to give 3-(4-tert-butyloxycarbonylphenyl)propionic acid ethyl ester.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customThe catalyst was removed by filtration
  • washwashed with ethanol
  • customThe combined solution was evaporated
  • 출처 및 근거

    ORD 기록
    ord-f068d433740847b5ac8ad7a6e65cb2dc
    출처 데이터셋
    uspto-grants-1988_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04742052

    반응 노트

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