Water → 2-Bromo-5-chloroaniline

HRID 1868810Notes

Reaction equation

HRID 1868810 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[N+:9]([O-])=O.O.[Cl-].[NH4+]>CO.[Fe]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[NH2:9]

Participants

6

Conditions

Temperature
23 °C

Procedure

A solution of 1-bromo-4-chloro-2-nitrobenzene (13.92 g, 58.87 mmol) in MeOH (300 mL) was treated with water (50 mL), ammonium chloride (22.99 g, 429.8 mmol), and iron powder (325 mesh, 16.44 g, 294.4 mmol). The suspension was stirred at 23° C. After 18 hours, the suspension was filtered through celite. The filter cake was washed with MeOH (500 mL). The combined filtrate/washings were concentrated, partitioned in EtOAc/water (500 mL/200 mL), and the organic layer was separated. The aqueous layer was washed with EtOAc (2×200 mL). The organic layers were combined, washed with brine (200 mL), dried (MgSO4), and concentrated in vacuo affording 11.51 g of 2-bromo-5-chlorobenzenamine.

Workup

  1. filtrationthe suspension was filtered through celite
  2. washThe filter cake was washed with MeOH (500 mL)
  3. concentrationThe combined filtrate/washings were concentrated
  4. custompartitioned in EtOAc/water (500 mL/200 mL)
  5. customthe organic layer was separated
  6. washThe aqueous layer was washed with EtOAc (2×200 mL)
  7. washwashed with brine (200 mL)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-6065449a28b549aeb2851f885813a023
Source dataset
uspto-grants-2009_12
Patent number
US07635715B2

Reaction notes

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