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

Carbon Dioxide → (1-Butyl-2-oxo-1,2-dihydropyridin-4-yl)acetic acid

HRID 733339
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 733339
[NH:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]1=[O:7].[Li+].[CH3:9]C([N-]C(C)C)C.[C:16](=[O:18])=[O:17].Cl.[CH2:20]1[CH2:24]O[CH2:22][CH2:21]1>>[CH2:22]([N:1]1[CH:6]=[CH:5][C:4]([CH2:9][C:16]([OH:18])=[O:17])=[CH:3][C:2]1=[O:7])[CH2:21][CH2:20][CH3:24]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 280Carbon DioxideHCID 313Hydrochloric AcidHCID 8028Tetrahydrofuran2×HCID 88712-PyridoneHCID 2724682Lithium diisopropylamide

Produkt 1

HCID 53429105(1-Butyl-2-oxo-1,2-dihydropyridin-4-yl)acetic acidAusbeute 66 %

Versuchsvorschrift

A solution of pyridinone ix (1.7 g, 10.3 mmol) in 20 mL anhydrous THF is added dropwise to a solution of LDA (2 M, 5.7 mL, 6.05 mmol) in 40 mL anhydrous THF at −78° C. The solution is allowed to stir for 45 minutes followed by the addition of solid CO2 (10 g). After 0.5 h the mixture is poured onto H2O and acidified with 1 N HCl. The solution is concentrated under reduced pressure and extracted with ethyl acetate and CH2Cl2. The combined organics are dried over MgSO4, filtered and concentrated to give a solid which is purified by flash chromatography (9/1:CH2Cl2/MeOH) to provide x as a white solid (1.4 g, 66%). (MS: M+H: 210.0).

Aufarbeitung

  1. additionAfter 0.5 h the mixture is poured onto H2O
  2. concentrationThe solution is concentrated under reduced pressure
  3. extractionextracted with ethyl acetate and CH2Cl2
  4. dry with materialThe combined organics are dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give a solid which
  8. customis purified by flash chromatography (9/1:CH2Cl2/MeOH)

Quellen und Nachweise

ORD-Eintrag
ord-dc9e87da64d34b028dde1b40045116c7
Quelldatensatz
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07589094B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion