Sulfuric Acid → 4-Iodo-3-methylbenzoic acid

HRID 1275621Notes

Reaction equation

HRID 1275621 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1N)[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:21].[K+]>O.C(OCC)(=O)C.[Cu](I)I>[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[I:21])[C:5]([OH:7])=[O:6]

Participants

8

Procedure

20 g (0.132 mol) of 3-methyl-4-aminobenzoic acid and 175 ml of sulfuric acid (20%) were introduced into a three-necked flask. A solution of 11.9 g (0.172 mmol) of sodium nitrite in 50 ml of water was added dropwise at -10° C. and the mixture was stirred for 2 hours. This solution was introduced dropwise, via a funnel cooled at -5° C., into a solution of 35 g (0.211 mol) of potassium iodide, 35.2 g (0.185 mol) of copper iodide and 175 ml of sulfuric acid (20%). The mixture was stirred for 8 hours, the reaction medium filtered, the solid obtained dissolved in ethyl acetate, washed with water and then with a solution of sodium sulfite, dried over magnesium sulfate and evaporated. 24.4 g (70%) of 3-methyl-4-iodobenzoic acid of melting point 205-10° C. were recovered.

Workup

  1. additionThis solution was introduced dropwise, via a funnel
  2. stirringThe mixture was stirred for 8 hours
  3. customthe reaction medium filtered, the solid obtained
  4. washwashed with water
  5. dry with materialwith a solution of sodium sulfite, dried over magnesium sulfate
  6. customevaporated
  7. custom24.4 g (70%) of 3-methyl-4-iodobenzoic acid of melting point 205-10° C. were recovered

Sources & evidence

ORD record
ord-e6d3ccaf66374d29b59e6c1f7c9ad1d3
Source dataset
uspto-grants-2000_12
Patent number
US06162815

Reaction notes

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