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Acetic Acid → 4-Bromo-3-chloro-5-methylaniline

HRID 1755011
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1755011
C(O)(=O)C.[Br:5][C:6]1[C:11]([CH3:12])=[CH:10][C:9]([N+:13]([O-])=O)=[CH:8][C:7]=1[Cl:16].O.C(=O)(O)[O-].[Na+]>C(O)C.[Fe]>[Br:5][C:6]1[C:11]([CH3:12])=[CH:10][C:9]([NH2:13])=[CH:8][C:7]=1[Cl:16]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 962WaterHCID 516892Sodium BicarbonateHCID 218863692-Bromo-1-chloro-3-methyl-5-nitrobenzene

Produkt 1

HCID 668171834-Bromo-3-chloro-5-methylanilineAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925
Iron
Katalysator
HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Iron (2.34 g, 41.8 mmol) and acetic acid (0.80 mL, 14.0 mmol) were added to a mixed solution of 2-bromo-1-chloro-3-methyl-5-nitro-benzene (3.50 g, 14.0 mmol) in ethanol (15 mL)-water (31 mL) at room temperature. The mixture was stirred at 100° C. for one hour, and a saturated aqueous sodium bicarbonate solution was then added at 0° C. The mixture was filtered through celite, and the filtrate was washed with ethyl acetate and water. The filtrate was concentrated under reduced pressure. Ethyl acetate was then added, and the organic layer and the aqueous layer were separated. The aqueous layer was repeatedly extracted with ethyl acetate three times, and the organic layers were then dried over sodium sulfate. The resulting residue was concentrated under reduced pressure to give 4-bromo-3-chloro-5-methyl-phenylamine as a pale brown solid (3.01 g, 98%).

Aufarbeitung

  1. filtrationThe mixture was filtered through celite
  2. washthe filtrate was washed with ethyl acetate and water
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. additionEthyl acetate was then added
  5. customthe organic layer and the aqueous layer were separated
  6. extractionThe aqueous layer was repeatedly extracted with ethyl acetate three times
  7. dry with materialthe organic layers were then dried over sodium sulfate
  8. concentrationThe resulting residue was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-2282d8a8bb24435a8e0969d8d7e249a5
Quelldatensatz
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09169254B2

Notizen zur Reaktion

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