1,1-Dibromoethane → 1-(2-Bromoethoxy)-3,5-dichlorobenzene

HRID 480291Notes

Reaction equation

HRID 480291 reaction equation
[OH-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]([OH:11])[CH:7]=[C:8]([Cl:10])[CH:9]=1.[Br:12][CH:13](Br)[CH3:14]>O.CCOC(C)=O>[Br:12][CH2:13][CH2:14][O:11][C:6]1[CH:5]=[C:4]([Cl:3])[CH:9]=[C:8]([Cl:10])[CH:7]=1

Participants

6

Procedure

To a solution of NaOH (2.45 g, 61.3 mmol) in water (20 mL) was added 3,5-dichlorophenol (5 g, 30.7 mmol). The solution was heated at reflux for 1 h and was cooled to room temperature. Dibromoethane (11.52 g, 61.3 mmol) was added and the reaction was heated at reflux for 24 h. The cooled solution was diluted with EtOAc and the organic solution was washed sequentially with HCl (1N, 1×), water (1×), and brine (1×). The organic solution was dried (MgSO4), filtered, and concentrated. Purification by flash chromatography (hexanes to 5% EtOAc in hexanes ) provided the title compound (3.79 g). 1H NMR (400 MHz, CDCl3) δ 6.98 (m, 1H), 6.82 (m, 2H), 4.25 (t, 2H), 3.61 (t, 2H).

Workup

  1. temperatureThe solution was heated
  2. temperatureat reflux for 1 h
  3. temperaturethe reaction was heated
  4. temperatureat reflux for 24 h
  5. washthe organic solution was washed sequentially with HCl (1N, 1×), water (1×), and brine (1×)
  6. dry with materialThe organic solution was dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customPurification by flash chromatography (hexanes to 5% EtOAc in hexanes )

Sources & evidence

ORD record
ord-596218c67fcc4a7899df65fa47efd1ad
Source dataset
uspto-grants-2003_11
Patent number
US06649657B2

Reaction notes

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