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Potassium Carbonate → Dimethyl 2-bromo-1H-imidazole-4,5-dicarboxylate

HRID 1446039
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1446039
[Br:1]Br.[NH:3]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6]([C:12]([O:14][CH3:15])=[O:13])[N:5]=[CH:4]1.C(=O)([O-])[O-].[K+].[K+]>ClCCl.C(#N)C>[Br:1][C:4]1[NH:3][C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6]([C:12]([O:14][CH3:15])=[O:13])[N:5]=1
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Komponenten

6

Edukt 3

HCID 11430Potassium CarbonateHCID 24408BromineHCID 768101H-Imidazole-4,5-dicarboxylic acid, 4,5-dimethyl ester

Produkt 1

HCID 21947693Dimethyl 2-bromo-1H-imidazole-4,5-dicarboxylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6342AcetonitrileLösungsmittel
HCID 6344
Dichloromethane
Lösungsmittel
2×

Versuchsvorschrift

At ambient temperature 9.50 g (59.45 mmol) bromine were added dropwise to a solution of 9.90 g (53.76 mmol) dimethyl imidazole-4,5-dicarboxylate in 300 ml dichloromethane and 80 ml acetonitrile. 7.46 g (54.00 mmol) potassium carbonate was added, and the reaction mixture was stirred for 2 hours at ambient temperature. Then the dichloromethane was eliminated using the rotary evaporator and the residue was combined with a saturated solution of sodium chloride and sodium thiosulphate. It was extracted ten times with ethyl acetate, the organic extracts were dried over sodium sulphate and then the solvent was eliminated.

Aufarbeitung

  1. customthe rotary evaporator
  2. extractionIt was extracted ten times with ethyl acetate
  3. dry with materialthe organic extracts were dried over sodium sulphate

Quellen und Nachweise

ORD-Eintrag
ord-3a41866df5ba423e9ccafeb7693c5281
Quelldatensatz
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07667035B2

Notizen zur Reaktion

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