3-Furoic acid → 5-Bromofuran-3-carboxylic acid

HRID 2099542Notes

Reaction equation

HRID 2099542 reaction equation
[Br-:1].[Br-].[Br-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[O:22]1[CH:26]=[CH:25][C:24]([C:27]([OH:29])=[O:28])=[CH:23]1>C(O)(=O)C>[Br:1][C:26]1[O:22][CH:23]=[C:24]([C:27]([OH:29])=[O:28])[CH:25]=1

Participants

4

Conditions

Temperature
40 °C

Procedure

To a stirred solution of pyridinium tribromide (14.3 g, 44.6 mmoles) in acetic acid (20 ml) was added 3-furoic acid (5 g, 44.6 mmoles). The resulting mixture was heated at 40° C. for 16 hours. The acetic acid was evaporated; the residue was dissolved in dichloromethane (50 ml), washed with water (3×50 ml) and dried (MgSO4). The solvent was evaporated and the residue was purified by HPLC (gradient: 20% acetonitrile/80% water containing 0.1% trifluoroacetic acid to 80% acetonitrile/20% water at a rate of 1%/min) to afford 5-Bromo-furan-3-carboxylic acid (7) as a white solid. LC/MS System A; Rt=2.52 mins, m/z (ES−)=189/191 (M−H for C5H3BrO3).

Workup

  1. customThe acetic acid was evaporated
  2. dissolutionthe residue was dissolved in dichloromethane (50 ml)
  3. washwashed with water (3×50 ml)
  4. dry with materialdried (MgSO4)
  5. customThe solvent was evaporated
  6. customthe residue was purified by HPLC (gradient

Sources & evidence

ORD record
ord-a93b53fa218f43a1899c6713b3b9c53a
Source dataset
uspto-grants-2009_08
Patent number
US07569602B2

Reaction notes

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