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4-Bromoaniline → 4-Bromo-N,N-dibutylaniline

HRID 2066351
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2066351
Br[CH2:2][CH2:3][CH2:4][CH3:5].[Br:6][C:7]1[CH:13]=[CH:12][C:10]([NH2:11])=[CH:9][CH:8]=1.[OH-].[K+]>>[CH2:2]([N:11]([CH2:2][CH2:3][CH2:4][CH3:5])[C:10]1[CH:12]=[CH:13][C:7]([Br:6])=[CH:8][CH:9]=1)[CH2:3][CH2:4][CH3:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 78074-BromoanilineHCID 8002Butyl bromideHCID 14797Potassium Hydroxide

Produkt 1

HCID 131691524-Bromo-N,N-dibutylanilineAusbeute 43 %

Versuchsvorschrift

1-Bromobutane (41.1 g, 300 mmol), 4-bromoaniline (17.2 g, 100 mmol) and KOH (16.8 g, 300 mmol) were heated at reflux under nitrogen gas for about 18 hours. After cooling, the mixture was partitioned between water and hexane and the organic layer washed with water followed by brine. After drying over MgSO4 and filtering, the solvent was evaporated and the mixture distilled under reduced pressure. Distillate fractions collected between 25-100° C. and pressure of 360-210 mTorr contained a mixture of products and starting material. The fractions collected at 100-107° C. and 200 mTorr pressure afforded 12.1 g (43%) of pure product.

Aufarbeitung

  1. temperatureat reflux under nitrogen gas for about 18 hours
  2. temperatureAfter cooling
  3. customthe mixture was partitioned between water and hexane
  4. washthe organic layer washed with water
  5. dry with materialAfter drying over MgSO4
  6. filtrationfiltering
  7. customthe solvent was evaporated
  8. distillationthe mixture distilled under reduced pressure
  9. customcollected between 25-100° C.
  10. additiona mixture of products
  11. customThe fractions collected at 100-107° C.

Quellen und Nachweise

ORD-Eintrag
ord-abf5be9c8a984f5182ac79518f0c9d70
Quelldatensatz
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08293451B2

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