Bromine → 2-Amino-5-bromonicotinic acid

HRID 729853Notes

Reaction equation

HRID 729853 reaction equation
[NH2:1][C:2]1[N:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Br:11]Br>C(O)(=O)C>[NH2:1][C:2]1[N:10]=[CH:9][C:8]([Br:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]

Participants

4

Procedure

25.00 g (0.181 mol) of 2-aminonicotinic acid were dispersed in 100 ml of glacial acetic acid. To this suspension was added a solution of 12.0 ml (0.23 mol) of bromine in 50 ml of glacial acetic acid. The mixture was stirred at room temperature for 20 hours. The precipitate formed was filtered off and washed with 100 ml of glacial acetic acid in several portions until the filtrate remained colorless. The crude was dried by suction and crystallized from boiling methanol to afford 38.63 g (0.178 mol, 98% yield) of 2-amino-5-bromonicotinic acid as slightly greenish to off-white crystalline needles. 1H-NMR (d6-DMSO) d: 8.45 [1H] d, 8.34 [1H] d.; MS: m/z 217 [MH]+.

Workup

  1. customThe precipitate formed
  2. filtrationwas filtered off
  3. washwashed with 100 ml of glacial acetic acid in several portions until the filtrate
  4. customThe crude was dried by suction
  5. customcrystallized

Sources & evidence

ORD record
ord-8e6b2c890ab1494da340a0c8bdc0f711
Source dataset
uspto-grants-2009_09
Patent number
US07582637B2

Reaction notes

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