StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Tetrahydrofuran → 2-Ethyl-8-methoxyquinoline-5-carboxylic acid

HRID 2393087
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2393087
Br[C:2]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH2:14][CH3:15])=[N:7]2.[OH-:16].[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C]=O.[O:39]1[CH2:43]CCC1>O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[CH2:14]([C:6]1[CH:5]=[CH:4][C:3]2[C:2]([C:43]([OH:39])=[O:16])=[CH:11][CH:10]=[C:9]([O:12][CH3:13])[C:8]=2[N:7]=1)[CH3:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 8028TetrahydrofuranHCID 11776TriphenylphosphineHCID 14798Sodium HydroxideHCID 18979097HCID 18979097, VerbindungHCID 178418416HCID 178418416, Verbindung

Produkt 1

HCID 189790842-Ethyl-8-methoxyquinoline-5-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel

2
HCID 6102075Dichlorobis(triphenylphosphine)palladiumKatalysatorHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
105 °C

Versuchsvorschrift

A mixture of 5-bromo-2-ethyl-8-methoxyquinoline (3.3 g), sodium hydroxide (3.1 g, 46% solution in water), triphenylphosphine (0.22 g), and bis(triphenylphosphine)palladium (II) chloride (0.14 g) in tetrahydrofuran (14 ml) and water (7 ml) was stirred in a pressurised reaction vessel and charged with carbon monoxide to a pressure of 160 psi. The vessel was heated to 105° C. and stirred for 24 hours. The reaction was allowed to cool and depressurised. The mixture was filtered and the solid collected washed with tetrahydrofuran (2×10 ml). The solid was dissolved in hot methanol (10 ml) and water (10 ml), and the solution filtered to remove any remaining solids. The hot solution was treated with glacial acetic acid (2 ml) and cooled in ice. The resulting precipitate was filtered off and dried over silica gel under vacuum to afford the title compound as a white solid (0.44 g).

Aufarbeitung

  1. stirringstirred for 24 hours
  2. temperatureto cool
  3. filtrationThe mixture was filtered
  4. customthe solid collected
  5. washwashed with tetrahydrofuran (2×10 ml)
  6. dissolutionThe solid was dissolved in hot methanol (10 ml)
  7. filtrationwater (10 ml), and the solution filtered
  8. customto remove any remaining solids
  9. additionThe hot solution was treated with glacial acetic acid (2 ml)
  10. temperaturecooled in ice
  11. filtrationThe resulting precipitate was filtered off
  12. customdried over silica gel under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-a097b292da0942bc9f65e885f774f466
Quelldatensatz
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05804588

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion