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

Imidazole → 4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

HRID 745914
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 745914
[H-].[Na+].[NH:3]1[CH:7]=[CH:6][N:5]=[CH:4]1.Cl[CH2:9][CH2:10][O:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([NH2:18])=[O:17])=[CH:14][CH:13]=1>CN(C)C=O>[C:16]([C:15]1[CH:19]=[CH:20][C:12]([O:11][CH2:10][CH2:9][N:3]2[CH:7]=[CH:6][N:5]=[CH:4]2)=[CH:13][CH:14]=1)(=[O:17])[NH2:18]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 795ImidazoleHCID 24758Sodium hydrideHCID 135691714-(2-Chloroethoxy)benzamide

Produkt 1

HCID 135691774-(2-(1H-imidazol-1-yl)ethoxy)benzamideAusbeute 50,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Sodium hydride (14.4 g, 50% suspension in mineral oil) was added cautiously to a stirred and cooled solution of imidazole (20.4 g) in dry N,N-dimethylformamide (100 ml). After the initial vigorous reaction had subsided the mixture was heated to 100° C. for 10 minutes and then stirred at room temperature for a further 1 hour. A solution of 4-(2-chloroethoxy)benzamide (60.0 g) in the minimum volume of N,N-dimethylformamide was added and the mixture was heated at 100° C. for 5.5 hours. The solvent was evaporated and the residue was poured into water. The mixture was extracted several times with chloroform and the combined chloroform extracts were dried (MgSO4) and evaporated to give a mixture of oil and solid. The mixture was triturated with ether and the solid was collected and crystallised from a mixture of methanol and ethyl acetate to give 1-[2-(4-carbamoyl phenoxy)ethyl]imidazole (35.2 g), m.p. 148°-149° C. Found: C, 62.25; H, 5.61; N, 18.54. C12H13N3O2 requires: C, 62.32; H, 5.67; N, 18.17%.

Aufarbeitung

  1. customAfter the initial vigorous reaction
  2. stirringstirred at room temperature for a further 1 hour
  3. temperaturethe mixture was heated at 100° C. for 5.5 hours
  4. customThe solvent was evaporated
  5. additionthe residue was poured into water
  6. extractionThe mixture was extracted several times with chloroform
  7. dry with materialthe combined chloroform extracts were dried (MgSO4)
  8. customevaporated
  9. customto give
  10. additiona mixture of oil and solid
  11. customThe mixture was triturated with ether
  12. customthe solid was collected
  13. customcrystallised from a mixture of methanol and ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-7c2b13bb0a474eb7baaef75b8a7d143f
Quelldatensatz
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04602016

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion