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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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methyl 3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoate → Methyl 3-(1-methyl-1H-pyrazol-4-yl)propanoate

HRID 474550
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인쇄 미리보기

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HRID 474550 반응식
[CH3:1][N:2]1[CH:6]=[C:5](/[CH:7]=[CH:8]/[C:9]([O:11][CH3:12])=[O:10])[CH:4]=[N:3]1>C(O)C.[Pd]>[CH3:1][N:2]1[CH:6]=[C:5]([CH2:7][CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:4]=[N:3]1
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참가 물질

4

반응물 1

HCID 21936263methyl 3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoate

생성물 1

HCID 21936147Methyl 3-(1-methyl-1H-pyrazol-4-yl)propanoate수율 98%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

반응 조건

온도
40 °C

실험 절차

To a solution of methyl ((E)-Methyl 3-(1-methyl-1H-pyrazol-4-yl)acrylate (18 g, 108 mmol) in ethanol (300 ml) was added Pd/C (4 g, 37.6 mmol) at room temperature. The reaction mixture was stirred at 40° C. for 12 h under hydrogen. The reaction mixture was cooled to room temperature, then the solid was removed by filtration. The filtrate was concentrated in vacuo to give the title compound as colorless oil (17.8 g, 80% yield). LCMS: rt=1.27 min, [M+H+]=169

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe solid was removed by filtration
  3. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-adb994ab60df4673a3b0e5b7247ebc88
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637536B2

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