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Sulfuric Acid → 4-Iodo-3-methylbenzoic acid

HRID 861799
Notes
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Reaction equation

HRID 861799 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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 1118Sulfuric Acid2×HCID 4875Potassium IodideHCID 755984-Amino-3-methylbenzoic acidHCID 23668193Sodium Nitrite

Product 1

HCID 15173224-Iodo-3-methylbenzoic acid

Reagents, catalysts & solvents 3

HCID 83717Copper iodide
Catalyst
HCID 962WaterSolvent
HCID 8857Ethyl AcetateSolvent

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 mol) of sodium nitrite in 50 ml of water was added dropwise at -10° C. and stirring was carried out for two hours. This solution was introduced dropwise via a refrigerated dropping funnel at -50° 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%). Stirring was carried out for eight hours, the reaction mixture was filtered and the solid obtained was dissolved in ethyl acetate. Washing was carried out with water and then with a sodium sulfite solution, drying was carried out over magnesium sulfate and evaporation was carried out. 24.4 g (70%) of 3-methyl-4-iodobenzoic acid, with a melting point of 205°-210° C., were recovered.

Workup

  1. additionThis solution was introduced dropwise via
  2. customat -50° C.
  3. stirringStirring
  4. waitwas carried out for eight hours
  5. filtrationthe reaction mixture was filtered
  6. customthe solid obtained
  7. washWashing
  8. dry with materialwith a sodium sulfite solution, drying
  9. customwas carried out over magnesium sulfate and evaporation
  10. custom24.4 g (70%) of 3-methyl-4-iodobenzoic acid, with a melting point of 205°-210° C., were recovered

Sources & evidence

ORD record
ord-a3f775a5b75b4e0e9447ee9d5f9bbe11
Source dataset
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05716624

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes