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Sodium Hydroxide → ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylate

HRID 2233813
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2233813
[Br:1]N1C(=O)CCC1=O.[CH2:9]([C:11]1[NH:15][C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:13][CH:12]=1)[CH3:10].[OH-].[Na+]>C(Cl)Cl>[Br:1][C:12]1[CH:13]=[C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[NH:15][C:11]=1[CH2:9][CH3:10]
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Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 67184N-bromobutanimideHCID 597485Ethyl 5-ethyl-1H-pyrrole-2-carboxylate2×

Produkt 1

HCID 68580112ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylateAusbeute 68 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

N-Bromosuccinimide (5.86 g, 0.033 mol) was added to a solution of ethyl 5-ethyl-1H-pyrrole-2-carboxylate (Intermediate 12, 5.0 g, 0.03 mol) in DCM (85 ml) at 0° C., and the reaction was stirred for 30 minutes then poured to a chilled beaker containing 2 N NaOH (50 ml). The layers were separated and the aqueous layer was extracted with DCM (×3). The combined organic extracts were washed with water and brine, dried over magnesium sulfate and concentrated. The resultant dark brown solid was purified by flash chromatography (hexanes/EtOAc, 10:1) to give the title product as a white solid (5.0 g, 68%).

Aufarbeitung

  1. additionthen poured to a chilled beaker
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with DCM (×3)
  4. washThe combined organic extracts were washed with water and brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated
  7. customThe resultant dark brown solid was purified by flash chromatography (hexanes/EtOAc, 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-e135598ffb5446758f60c3f60b9e7749
Quelldatensatz
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07709503B2

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