Sodium Hydroxide → 4,5-Dibromobenzene-1,2-diamine

HRID 439457Notes

Reaction equation

HRID 439457 reaction equation
[Br:1][C:2]1[C:8]([Br:9])=[CH:7][C:5]([NH2:6])=[C:4]([N+:10]([O-])=O)[CH:3]=1.[OH-].[Na+]>CCOC(C)=O>[Br:1][C:2]1[C:8]([Br:9])=[CH:7][C:5]([NH2:6])=[C:4]([NH2:10])[CH:3]=1

Participants

4

Conditions

Temperature
75 °C

Procedure

To a solution of 4,5-dibromo-2-nitroaniline (3.35 g, 11.32 mmol) in EtOAc (150 mL) was added stannous chloride dihydrate (12.8 g, 56.74 mmol), the mixture was stirred at 75° C. for 16 h, then allowed to cool to room temperature and poured into ice-water (about 150 mL). To the mixture was added 1N aq NaOH with vigorous stirring to take the pH to 9 (pH paper). The resulting thick yellow white emulsion was extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with brine (2×50 mL), dried (over Na2SO4) and evaporated to dryness. The residual solid was dried under 1 mmHg at 40° C. for 14 h giving 2.92 g (97%) of 4,5-dibromo-1,2-phenylenediamine as a yellowish powder. Mp 149°-50° C. IR (KBr) 3400, 1623, 1489, 1394, 1271, 868 cm-1. 1H NMR (DMSO-d6) 6.754 (s, 2H), 4.867 (s, 4H).

Workup

  1. temperatureto cool to room temperature
  2. stirringwith vigorous stirring
  3. extractionThe resulting thick yellow white emulsion was extracted with EtOAc (3×100 mL)
  4. washwashed with brine (2×50 mL)
  5. dry with materialdried (over Na2SO4)
  6. customevaporated to dryness
  7. customThe residual solid was dried under 1 mmHg at 40° C. for 14 h

Sources & evidence

ORD record
ord-71974282c0cc43409a9c98be9271fbab
Source dataset
uspto-grants-1996_05
Patent number
US05514680

Reaction notes

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