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Potassium Carbonate → 2-Bromo-1-methoxy-4-(2-methoxy-ethoxy)-benzene

HRID 2097590
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2097590
[CH3:1][O:2][CH2:3][CH2:4]Br.C(=O)([O-])[O-].[K+].[K+].[Br:12][C:13]1[CH:14]=[C:15]([OH:21])[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]>CN(C=O)C>[Br:12][C:13]1[CH:14]=[C:15]([O:21][CH2:4][CH2:3][O:2][CH3:1])[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 809722-Bromoethyl methyl etherHCID 6088153-Bromo-4-methoxyphenol

Produkt 1

HCID 580730982-Bromo-1-methoxy-4-(2-methoxy-ethoxy)-benzeneAusbeute 88,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

2-bromoethyl methyl ether (0.07 mL, 0.74 mmol) was added to a mixture of potassium carbonate (136 mg, 0.99 mmol) and 3-bromo-4-methoxy-phenol (100 mg, 0.49 mmol) in DMF (2 mL) and mix heated at 100° C. for 1 hr. Reaction mixture was allowed to cool and partitioned between ethyl acetate (20 mL×2) and water (20 mL). The combined organic phases were washed with sat. aqueous sodium chloride solution (40 mL) and dried over sodium sulphate. Solvents were removed in vacuo to afford a crude oil which was purified by flash chromatography on silica gel, eluting with a gradient of 0-10% ethyl acetate in hexane to afford the title compound (113 mg, 88%) as a colourless liquid.

Aufarbeitung

  1. additionmix
  2. customReaction mixture
  3. temperatureto cool
  4. custompartitioned between ethyl acetate (20 mL×2) and water (20 mL)
  5. washThe combined organic phases were washed with sat. aqueous sodium chloride solution (40 mL)
  6. dry with materialdried over sodium sulphate
  7. customSolvents were removed in vacuo
  8. customto afford a crude oil which
  9. customwas purified by flash chromatography on silica gel
  10. washeluting with a gradient of 0-10% ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-252b91457904416e80633f727d9a2667
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08450346B2

Notizen zur Reaktion

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