Hydrogen Bromide → HCID 22387869, compound

HRID 1072916Notes

Reaction equation

HRID 1072916 reaction equation
[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4](Cl)[N:3]=1.[BrH:12]>Br.C(O)(=O)C>[BrH:12].[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4]([Br:12])[N:3]=1

Participants

4

Conditions

Temperature
90 °C

Procedure

2-Amino-6-chloro-3-nitropyridine (20.2 g) was suspended in a 30% hydrobromide/acetic acid solution (100 ml), and the suspension was stirred at 90° C. After 4 hours, a 30% hydrobromide/acetic acid solution (100 ml) was added, and the mixture was stirred for another 1 hour at 90° C. Then, the reaction mixture was stirred at 100° C. for 8 hr while a hydrobromic acid gas was introduced little by little. The reaction mixture was cooled, and the precipitate was collected by filtration and washed with hexane to give the objective compound (33.0 g) as a pale-yellow powder.

Workup

  1. stirringthe mixture was stirred for another 1 hour at 90° C
  2. additionwas introduced little by little
  3. temperatureThe reaction mixture was cooled
  4. filtrationthe precipitate was collected by filtration
  5. washwashed with hexane

Sources & evidence

ORD record
ord-758007d56a6347e9a035a1f2f749fb42
Source dataset
uspto-grants-2005_06
Patent number
US06911469B2

Reaction notes

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