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Quinoline → Methyl 5-ethenyl-2-hydroxybenzoate

HRID 742996
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 742996
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

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

Produkt 1

HCID 19423384Methyl 5-ethenyl-2-hydroxybenzoate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-f39397c1b12441b296724f0fb7e29ea9
Quelldatensatz
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05556855

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