Water → 5-Nitroindole

HRID 907127Notes

Reaction equation

HRID 907127 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH:8]=[CH:7]2)([O-:3])=[O:2].C1C=C[NH+]=CC=1.[Br:19][Br-]Br.O>N1C=CC=CC=1>[Br:19][C:7]1[C:6]2[C:10](=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[NH:9][CH:8]=1.[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH:8]=[CH:7]2)([O-:3])=[O:2]

Participants

5

Reactant 2

HCID 962WaterHCID 225235-Nitroindole

Product 2

HCID 225235-NitroindoleYield 272.3%HCID 431520843-Bromo-5-nitro-1H-indole

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent2×

Procedure

To a solution of 5-nitroindole (5.00 g, 30.8 mmol) in pyridine (200 mL) at −4° C. was added a solution of pyridinium bromide perbromide (10.99 g, 34.3 mmol) in pyridine (200 mL) dropwise under nitrogen with stirring. After complete addition, the reaction mixture was stirred for 5 min at 0° C. The reaction mixture was diluted in 0° C. water (200 mL) and extracted with 200 mL of Et2O. The organic layer was washed with 6 M HCl (300 mL), 5% NaHCO3 (300 mL), and brine (300 mL). The organic phase was dried over MgSO4 and solvent was removed to give 3-bromo-5-nitroindole as a yellow powder, 80% pure with 20% 5-nitroindole (6.80 g, 74% yield).

Workup

  1. additionAfter complete addition
  2. stirringthe reaction mixture was stirred for 5 min at 0° C
  3. extractionextracted with 200 mL of Et2O
  4. washThe organic layer was washed with 6 M HCl (300 mL), 5% NaHCO3 (300 mL), and brine (300 mL)
  5. dry with materialThe organic phase was dried over MgSO4 and solvent
  6. customwas removed

Sources & evidence

ORD record
ord-62f0c1429cab4e4aa72b97e3ff3b401d
Source dataset
uspto-grants-2011_09
Patent number
US08013006B2

Reaction notes

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