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Potassium Carbonate → Methyl 5-bromo-3-methylbenzofuran-2-carboxylate

HRID 2091390
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091390
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([C:8](=O)[CH3:9])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:19][C:20]([O:22][CH3:23])=[O:21]>CN(C)C=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:11][C:19]([C:20]([O:22][CH3:23])=[O:21])=[C:8]([CH3:9])[C:6]=2[CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 60984Methyl bromoacetateHCID 959915'-Bromo-2'-hydroxyacetophenone

Produkt 1

HCID 42967109Methyl 5-bromo-3-methylbenzofuran-2-carboxylateAusbeute 52 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution (200 mL) of 1-(5-bromo-2-hydroxyphenyl)ethanone (25.0 g) in N,N-dimethylformamide were added potassium carbonate (24.0 g) and methyl bromoacetate (11.5 mL) at room temperature, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was filtered, 1,8-diazabicyclo[5.4.0]undec-7-ene (23.2 mL) was added to the filtrate, and the mixture was stirred at 100° C. for 3 hr. The reaction mixture was allowed to cool to room temperature, and ice water was added. The precipitate was washed with ethanol-water to give the title object compound (16.8 g, 52%) as a pale-red solid.

Aufarbeitung

  1. filtrationThe reaction mixture was filtered
  2. addition1,8-diazabicyclo[5.4.0]undec-7-ene (23.2 mL) was added to the filtrate
  3. stirringthe mixture was stirred at 100° C. for 3 hr
  4. temperatureto cool to room temperature
  5. additionice water was added
  6. washThe precipitate was washed with ethanol-water

Quellen und Nachweise

ORD-Eintrag
ord-77ebe215a9c14134a128ad2acfd525cf
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08436043B2

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