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

Bis-(1H-imidazol-2-YL)-methanone → (R)-(-)-5,5-Dimethyl-4-phenyl-2-oxazolidinone

HRID 2392834
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2392834
[NH2:1][C@H:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:3]([CH3:6])([OH:5])[CH3:4].[C:13](C1NC=CN=1)(C1NC=CN=1)=[O:14]>ClCCl>[C:7]1([C@@H:2]2[C:3]([CH3:6])([CH3:4])[O:5][C:13](=[O:14])[NH:1]2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 5250894Bis-(1H-imidazol-2-YL)-methanoneHCID 11240681(βR)-β-Amino-α,α-dimethylbenzeneethanol

Produkt 1

HCID 6950851(R)-(-)-5,5-Dimethyl-4-phenyl-2-oxazolidinoneAusbeute 82,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of (13) (1.30 g, 7.89 mmol) in dichloromethane (100 ml) was added carbonyl diimidazole (1.534 g, 9.47 mmol) and the reaction mixture was refluxed for 2 hours. The reaction was quenched with hydrochloric acid (1M) and the product extracted repeatedly with dichloromethane. The combined organic extracts were dried over magnesium sulphate. After concentration in vacuo the residue was purified by flash column chromatography using 40% ethyl acetate/40-60 petroleum ether as eluant to give the title compound (15) (1.24 g, 82%).

Aufarbeitung

  1. temperaturethe reaction mixture was refluxed for 2 hours
  2. customThe reaction was quenched with hydrochloric acid (1M)
  3. extractionthe product extracted repeatedly with dichloromethane
  4. dry with materialThe combined organic extracts were dried over magnesium sulphate
  5. concentrationAfter concentration in vacuo the residue
  6. customwas purified by flash column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-2b20d07d42ed4c48b8d5920618b96d1c
Quelldatensatz
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05801249

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion