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Methanol → methyl 3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoate

HRID 474549
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HRID 474549 반응식
[CH3:1][N:2]1[CH:6]=[C:5](/[CH:7]=[CH:8]/[C:9]([OH:11])=[O:10])[CH:4]=[N:3]1.OS(O)(=O)=O.[OH-].[Na+].[CH3:19]O>>[CH3:1][N:2]1[CH:6]=[C:5](/[CH:7]=[CH:8]/[C:9]([O:11][CH3:19])=[O:10])[CH:4]=[N:3]1
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참가 물질

5

반응물 4

HCID 887MethanolHCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 1529858(2E)-3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoic acid

생성물 1

HCID 21936263methyl 3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoate수율 71.8%

실험 절차

(2E)-3-(1-Methyl-1H-pyrazol-4-yl)-2-propenoic acid (7.5 g, 49.3 mmol) was added to a solution of H2SO4 (1.760 ml, 33.0 mmol) in methanol (40 ml), and the resultant mixture was refluxed for 4 h. It was cooled to room temperature, then poured into ice. The acid was neutralized with aqueous sodium hydroxide and extracted with DCM (80 ml×2). The organic phases were collected and combined, dried over MgSO4, and concentrated. The residue was washed with petroleum ether and concentrated to give the title compound (7 g, 71.8% yield). LCMS: rt=1.13 min, [M+H+]=167

후처리

  1. additionpoured into ice
  2. extractionextracted with DCM (80 ml×2)
  3. customThe organic phases were collected
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. washThe residue was washed with petroleum ether
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6f9d6c8a9375495f8baaac15e14197b8
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637536B2

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