Sodium Hydroxide → 4-Bromo-N1-methylbenzene-1,2-diamine

HRID 643404

Reaktionsgleichung

Reaktionsgleichung von HRID 643404
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-])=O)[CH:3]=1.O.O.Cl[Sn]Cl.[OH-].[Na+]>CCO>[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH:6][CH3:7])=[CH:8][CH:9]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A suspension of 4-bromo-N-methyl-2-nitroaniline (5328 mg, 22.04 mmol) in EtOH (100 ml) was treated with SnCl2.2H2O (25.61 g, 110.2 mmol) and the resulting mixture heated at 70° C. under an atmosphere of Nitrogen for 5 h. The reaction mixture was then cooled to rt and treated with ice-water (50 ml) followed by aqueous NaOH (4 N) until pH>8. This basic mixture was then extracted with EtOAc (3×150 ml) and the combined extracts washed with brine (3×100 ml), dried over MgSO4 and concentrated in vacuo to afford the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm=2.68 (s, 3H), 4.74 (brs, 3H), 6.27 (d, 1H, J=8.4 Hz), 6.61 (dd, 1H, J=2.0 & 8.4 Hz) and 6.66 (d, 1H, J=2.0 Hz). MS(ES+): m/z 201.10 and 203.12[MH+].

Aufarbeitung

  1. temperatureThe reaction mixture was then cooled to rt
  2. extractionThis basic mixture was then extracted with EtOAc (3×150 ml)
  3. washthe combined extracts washed with brine (3×100 ml)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-db0dc43dba664a669abf928b24912f5f
Quelldatensatz
uspto-grants-2010_04
Patentnummer
US07700594B2

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