2-Fluoroaniline → 4-Bromo-2-fluoroaniline

HRID 1076922Notes

Reaction equation

HRID 1076922 reaction equation
[Br:1]N1C(=O)CCC1=O.[F:9][C:10]1[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=1[NH2:12]>C(Cl)Cl>[Br:1][C:15]1[CH:14]=[CH:13][C:11]([NH2:12])=[C:10]([F:9])[CH:16]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

160 Parts of solid N-bromosuccinimide were added in portions over a 2 hour period to a solution of 100 parts of 2-fluoroaniline in 400 parts of methylene chloride cooled to 0°C. After stirring for 20 minutes, the dark red mixture was washed 4 times; 200 parts of cold water were used for each washing. The red organic phase was dried with anhydrous sodium sulfate and evaporated under 300 mm Hg. to 164 parts of brown, oily 4-bromo-2-fluoroaniline, nD25 : 1.5885.

Workup

  1. washthe dark red mixture was washed 4 times
  2. dry with materialThe red organic phase was dried with anhydrous sodium sulfate
  3. customevaporated under 300 mm Hg

Sources & evidence

ORD record
ord-a810249541854d8e90073773641e3d6d
Source dataset
uspto-grants-1976_05
Patent number
US03958976

Reaction notes

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