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

Benzene → HCID 22010727, Verbindung

HRID 323133
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 323133
[N+:1]([C:4]1[CH:22]=[CH:21][C:7]([C:8]([N:10]([CH3:20])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][CH2:18][OH:19])=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.C1C=CC=CC=1.C[Si](C=[N+]=[N-])(C)C.CN(C)[CH:59]=[O:60]>O.CO>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:8]([N:10]([CH3:20])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][C:18]([O:60][CH3:59])=[O:19])=[O:9])=[CH:21][CH:22]=1)([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 241BenzeneHCID 6228DimethylformamideHCID 167693TrimethylsilyldiazomethaneHCID 2724130Cornforth reagentHCID 22010650HCID 22010650, Verbindung

Produkt 1

HCID 22010727HCID 22010727, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel

2
HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution of 4-nitro-N-methyl-N-[2-(2-hydroxyethyl)phenyl]benzamide (686 mg) in N,N-dimethylformamide (12 ml) was added pyridinium dichromate (4.3 g) and the mixture was stirred at ambient temperature for 2 days. The mixture was diluted with water (80 ml) and the aqueous solution was extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate. Filtering and removal of solvents afforded a brown oil. To a solution of the brown oil in methanol (3 ml) and benzene (11 ml) was added trimethylsilyl diazomethane (1.7 ml) and the resulting solution was stirred at ambient temperature for 30 minutes. The mixture was evaporated in vacuo to give 4-nitro-N-methyl-N-(2-methoxycarbonylmethylphenyl)benzamide (517 mg) as a dark-green oil.

Aufarbeitung

  1. extractionthe aqueous solution was extracted with ethyl acetate
  2. washThe extract was washed with brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationFiltering
  5. customremoval of solvents
  6. customafforded a brown oil
  7. stirringthe resulting solution was stirred at ambient temperature for 30 minutes
  8. customThe mixture was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ba858072efd54647886a5c18e2ff1fb7
Quelldatensatz
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06211242B1

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion