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Quinoline → Methyl 5-ethenyl-2-hydroxybenzoate

HRID 742996
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HRID 742996 반응식
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([OH:13])=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9])#[CH:2].N1C2C(=CC=CC=2)C=CC=1>C(OCC)C.[Pd]>[CH:1]([C:3]1[CH:4]=[CH:5][C:6]([OH:13])=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9])=[CH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7047QuinolineHCID 14172485Methyl 5-ethynyl-2-hydroxybenzoate

생성물 1

HCID 19423384Methyl 5-ethenyl-2-hydroxybenzoate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 3283Diethyl Ether용매

실험 절차

Methyl 5-ethynyl-2-hydroxybenzoate (8 g, 45.4 mmol), prepared according to Example 1 b, was dissolved in a mixture of diethyl ether and light petroleum (200+200 ml) in a hydrogenation flask. Quinoline (1.7 ml) and palladium on CaCO3, poisoned with Pb (Lindlax catalyst; 200 mg) were added, and the flask was attached to an atmospheric pressure hydrogenation apparatus. The mixture was stirred for 2 h at room temperature, by then the calculated amount of hydrogen had been consumed. The catalyst was filtered off and the solution was evaporated to dryness. The product was purified by flash column chromatograpy on silica, using toluene as an eluent. A nearly quantitative yield was obtained.

후처리

  1. additionwere added
  2. customby then the calculated amount of hydrogen had been consumed
  3. filtrationThe catalyst was filtered off
  4. customthe solution was evaporated to dryness
  5. customThe product was purified by flash column chromatograpy on silica
  6. customA nearly quantitative yield was obtained

출처 및 근거

ORD 기록
ord-f39397c1b12441b296724f0fb7e29ea9
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556855

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