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5-Bromo-1-methoxy-2-methyl-3-nitrobenzene → 5-Bromo-3-methoxy-2-methylaniline

HRID 1889252
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1889252
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[C:5]([CH3:11])=[C:4]([O:12][CH3:13])[CH:3]=1>[Fe].C(O)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([O:12][CH3:13])[C:5]([CH3:11])=[C:6]([CH:7]=1)[NH2:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 247281025-Bromo-1-methoxy-2-methyl-3-nitrobenzene

Produkt 1

HCID 272747255-Bromo-3-methoxy-2-methylaniline

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

A heterogeneous reaction mixture of 4-bromo-2-methoxy-6-nitrotoluene (500 mg, 2.032 mmol), acetic acid (20 ml), and iron (1135 mg, 20.32 mmol) was stirred at rt for 24 hr. Ethyl actetate was added, then the mixture was filtered through celite and the filtrate concentrated. The residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The aqueous layer was extracted with further ethyl acetate. The combined organic phases were washed with water and brine, then dried over sodium sulfate, filtered and concentrated to afford the title compound. MS m/z: 218.0 (M+H)+.

Aufarbeitung

  1. additionEthyl actetate was added
  2. filtrationthe mixture was filtered through celite
  3. concentrationthe filtrate concentrated
  4. customThe residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution
  5. extractionThe aqueous layer was extracted with further ethyl acetate
  6. washThe combined organic phases were washed with water and brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-32bcf6637b00428bb7888de31e4d53f8
Quelldatensatz
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08501758B2

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