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

Potassium Carbonate → 1-(4-(2-Hydroxyethyl)phenyl)pyrrolidin-2-one

HRID 1023887
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1023887
CN(CC)C.C([O-])([O-])=O.[K+].[K+].[NH:12]1[CH2:16][CH2:15][CH2:14][C:13]1=[O:17].Br[C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][OH:27])=[CH:21][CH:20]=1>[Cu]I>[OH:27][CH2:26][CH2:25][C:22]1[CH:23]=[CH:24][C:19]([N:12]2[CH2:16][CH2:15][CH2:14][C:13]2=[O:17])=[CH:20][CH:21]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 11430Potassium CarbonateHCID 11723DimethylethylamineHCID 120252-PyrrolidoneHCID 728512-(4-Bromophenyl)ethanol

Produkt 1

HCID 214891281-(4-(2-Hydroxyethyl)phenyl)pyrrolidin-2-oneAusbeute 37 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Katalysator

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

A mixture of CuI (0.198 mmol), N,N-dimethylethylamine (0.398 mmol), K2CO3 (3.98 mmol) and pyrrolidin-2-one (3.98 mmol) was purged with nitrogen gas. 2-(4-bromophenyl)ethanol (1.99 mmol) was added and the mixture was purged with purged again with nitrogen. The reaction mixture was stirred at 130° C. overnight. After cooling to room temperature, the reaction mixture was diluted with water (25 mL), NH4OH (5 mL) and the aqueous layer was extracted with dichloromethane (3×40 mL). The combined organic extracts were dried over sodium sulfate and evaporated under reduced pressure; the crude was purified by column chromatography to afford the final product. Yield=37%.

Aufarbeitung

  1. customwas purged with nitrogen gas
  2. customthe mixture was purged
  3. customwith purged again with nitrogen
  4. temperatureAfter cooling to room temperature
  5. additionthe reaction mixture was diluted with water (25 mL), NH4OH (5 mL)
  6. extractionthe aqueous layer was extracted with dichloromethane (3×40 mL)
  7. dry with materialThe combined organic extracts were dried over sodium sulfate
  8. customevaporated under reduced pressure
  9. customthe crude was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-cac7aea0fdfc45639101761658c312fb
Quelldatensatz
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08722720B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion