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2-[2-(4-Bromophenyl)ethoxy]ethanol → HCID 13208939, Verbindung

HRID 2078424
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2078424
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][OH:13])=[CH:4][CH:3]=1.[C:14]([Cu])#[N:15]>CN(C=O)C>[C:14]([C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][OH:13])=[CH:4][CH:3]=1)#[N:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 691375802-[2-(4-Bromophenyl)ethoxy]ethanolHCID 178418546HCID 178418546, Verbindung

Produkt 1

HCID 13208939HCID 13208939, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
145 °C

Versuchsvorschrift

To a solution of 2-[2-(4-bromophenyl)ethoxy]ethanol (10.8 g, 0.044 mol; see step (iii) above in DMF (100 mL), CuCN (7.8 g, 0.088 mol) was added and refluxed at 140 to 150° C. overnight. After removal of DMF by distillation, the reaction was quenched by the addition of water. Inorganic matter was removed by filtration and the aqueous layer was extracted with ethyl acetate (4×100 mL). The combined organic layers were washed with water and brine before being concentrated. The crude product was purified by column chromatography (silica gel: 60-120 mesh, petroleum ether:ethyl acetate (75:25) eluent). This yielded 4.3 g (51%) of the sub-title compound.

Aufarbeitung

  1. additionwas added
  2. customAfter removal of DMF
  3. distillationby distillation
  4. customthe reaction was quenched by the addition of water
  5. customInorganic matter was removed by filtration
  6. extractionthe aqueous layer was extracted with ethyl acetate (4×100 mL)
  7. washThe combined organic layers were washed with water and brine
  8. concentrationbefore being concentrated
  9. customThe crude product was purified by column chromatography (silica gel: 60-120 mesh, petroleum ether:ethyl acetate (75:25) eluent)

Quellen und Nachweise

ORD-Eintrag
ord-59c8650abae344b583af1331eaf069b7
Quelldatensatz
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07928225B2

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