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1,10-Phenanthroline → 2-(3-Bromophenyl)benzoxazole

HRID 2170602
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2170602
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](Cl)=[O:6].Br[C:12]1[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=1[NH2:14].C([O-])([O-])=O.[Cs+].[Cs+].N1C2C(=CC=C3C=2N=CC=C3)C=CC=1>[Cu]I.O1CCOCC1>[Br:1][C:2]1[CH:3]=[C:4]([C:5]2[O:6][C:12]3[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=3[N:14]=2)[CH:8]=[CH:9][CH:10]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 13181,10-PhenanthrolineHCID 10796Cesium carbonateHCID 119922-BromoanilineHCID 74377Benzoyl chloride, 3-bromo-

Produkt 1

HCID 8705202-(3-Bromophenyl)benzoxazoleAusbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Katalysator
HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

A mixture of 3-bromobenzoyl chloride (6.005 g, 27.36 mmol), 2-bromoaniline (4.707 g, 27.36 mmol), Cs2CO3 (17.83 g, 54.73 mmol), CuI (0.261 g, 1.37 mmol), 1,10-phenanthroline (0.493 g, 2.74 mmol) and anhydrous 1,4-dioxane (50 mL) was degassed with argon at 40° C. for 30 min while stirring. The reaction mixture was then maintained under argon at 120° C. while stirring until TLC (SiO2, 4:1 hexanes-ethyl acetate) confirmed consumption of the starting material (24 h). Upon cooling to RT, the mixture was filtered and the filtrant washed copiously with ethyl acetate (ca. 350 mL). The filtrate was then washed with sat. NaHCO3, H2O and brine, dried over MgSO4, filter and concentrated in vacuo. Purification of the crude product via flash chromatography (SiO2, 4:1-hexanes:ethyl acetate) afforded 2-(3-bromophenyl)benzo[d]oxazole (7.50 g, 100%) as an off-white solid.

Aufarbeitung

  1. customwas degassed with argon at 40° C. for 30 min
  2. stirringwhile stirring until TLC (SiO2, 4:1 hexanes-ethyl acetate)
  3. customconsumption of the starting material (24 h)
  4. temperatureUpon cooling to RT
  5. filtrationthe mixture was filtered
  6. washthe filtrant washed copiously with ethyl acetate (ca. 350 mL)
  7. washThe filtrate was then washed with sat. NaHCO3, H2O and brine
  8. dry with materialdried over MgSO4
  9. filtrationfilter
  10. concentrationconcentrated in vacuo
  11. customPurification of the crude product via flash chromatography (SiO2, 4:1-hexanes:ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-40eeae8cc7ee4c2b9c8cc49a4cfbd4d1
Quelldatensatz
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09051284B2

Notizen zur Reaktion

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