Hydrochloric Acid → 5-Bromo-4-fluoro-2-iodobenzoic acid
Reaction equation
S(=O)(=O)(O)O.N[C:7]1[CH:15]=[C:14]([F:16])[C:13]([Br:17])=[CH:12][C:8]=1[C:9]([OH:11])=[O:10].Cl.[N+]([O-])([O-])=O.[Na+].[I-:24].[K+]>O.CCOC(C)=O>[Br:17][C:13]1[C:14]([F:16])=[CH:15][C:7]([I:24])=[C:8]([CH:12]=1)[C:9]([OH:11])=[O:10]Participants
Procedure
Sulfuric acid (19.36 mL, 363 mmol) was added to a solution of 2-amino-5-bromo-4-fluorobenzoic acid (5.00 g, 21.37 mmol) in concentrated HCl (5.13 mL, 64.1 mmol) at 0° C. To this was added a solution of sodium nitrate (1.816 g, 21.37 mmol) in water (9 mL). The reaction was stirred for 40 minutes at 0° C. before potassium iodide (7.09 g, 42.7 mmol) in water (9.00 mL) was added dropwise. The solution was stirred at rt for 1 hour, at which point it had become a viscous oil. The mixture was poured into a mixture of ice water (250 mL) with EtOAc (200 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×100 mL). The combined organic extracts were washed with 1N HCl, 1 N aqueous sodium sulfite, and dried over sodium sulfate. The solution was filtered and concentrated in vacuo to give 5-bromo-4-fluoro-2-iodobenzoic acid.
Workup
- additionwas added dropwise
- customThe layers were separated
- extractionthe aqueous layer was extracted with EtOAc (3×100 mL)
- washThe combined organic extracts were washed with 1N HCl, 1 N aqueous sodium sulfite
- dry with materialdried over sodium sulfate
- filtrationThe solution was filtered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-7b44eb6e0a774e53bfe9a59c1cbda9b9
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08883782B2
Reaction notes
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