Lithium Hydroxide → 5-Bromo-1H-indole-7-carboxylic acid

HRID 562010Notes

Reaction equation

HRID 562010 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([O-:13])=[O:12])[CH:10]=1)[NH:7][CH:6]=[CH:5]2.[OH-].[Li+]>CO.O>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([OH:13])=[O:12])[CH:10]=1)[NH:7][CH:6]=[CH:5]2

Participants

5

Reactant 2

HCID 3939Lithium HydroxideHCID 863070595-bromo-1H-indole-7-carboxylate

Product 1

HCID 533992575-Bromo-1H-indole-7-carboxylic acidYield 99.4%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

5-bromo-1H-indole-7-carboxylate (5 g, 19.7 mmol) was dissolved in methanol (200 mL) and a solution of lithium hydroxide (0.99 g, 41 mmol) in water (10 mL) was added. The mixture was heated at reflux for 50 hours. The methanol was removed in vacuo and the residue diluted with aqueous hydrochloric acid (2 M). The resulting precipitate was filtered off and dried in a heated vacuum pistol to give the title compound as a beige solid (4.7 g).

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 50 hours
  3. customThe methanol was removed in vacuo
  4. additionthe residue diluted with aqueous hydrochloric acid (2 M)
  5. filtrationThe resulting precipitate was filtered off
  6. customdried in a heated vacuum pistol

Sources & evidence

ORD record
ord-ee414f30ad24476bb722c802d1c40d8e
Source dataset
uspto-grants-2011_11
Patent number
US08063071B2

Reaction notes

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