Chloroform → 4-Bromo-2-fluoroanisole

HRID 2372253Notes

Reaction equation

HRID 2372253 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].C(Cl)(Cl)Cl.[Br:14]Br.S(=O)(O)[O-].[Na+]>O>[F:1][C:2]1[CH:7]=[C:6]([Br:14])[CH:5]=[CH:4][C:3]=1[O:8][CH3:9]

Participants

6

Conditions

Temperature
10 °C

Procedure

Into a flask of 5 l were charged 384 g (3.04 mol) of 2-fluoroanisole and 2.5 l of chloroform, to which was added dropwise 504 g (3.16 mol) of bromine over about 3 hours while cooling on an ice water bath at 10° C. The resulting mixture was stirred at room temperature over a night and heated under reflux for 8 hours. After the air cooling, the product was added with 1 l of water and 50 g of sodium bisulfite and sufficiently shaken to separate into two layers. The resulting organic layer was washed with an aqueous solution of 5% sodium hydrogen carbonate and further with 1 l of water and dried on magnesium sulfate. After magnesium sulfate was filtered off, the filtrate was concentrated and distilled under a reduced pressure (4 mmHg, bp: 93-°96° C.) to obtain 585 g (yield: 94%) of 3-fluoro-4-methoxybromobenzene.

Workup

  1. temperatureheated
  2. temperatureunder reflux for 8 hours
  3. temperatureAfter the air cooling
  4. stirringsufficiently shaken
  5. customto separate into two layers
  6. washThe resulting organic layer was washed with an aqueous solution of 5% sodium hydrogen carbonate and further with 1 l of water
  7. customdried on magnesium sulfate
  8. filtrationAfter magnesium sulfate was filtered off
  9. concentrationthe filtrate was concentrated
  10. distillationdistilled under a reduced pressure (4 mmHg, bp: 93-°96° C.)

Sources & evidence

ORD record
ord-b3562b5f82ae42299feec8bea0368ff5
Source dataset
uspto-grants-1992_03
Patent number
US05098602

Reaction notes

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