Iodine → 2-Iodo-4-(trifluoromethyl)phenol

HRID 1369466Notes

Reaction equation

HRID 1369466 reaction equation
[I:1]I.C(=O)(O)[O-].[Na+].[F:8][C:9]([F:18])([F:17])[C:10]1[CH:11]=[CH:12][C:13]([OH:16])=[CH:14][CH:15]=1.NC(N)=S>C1COCC1.O>[F:8][C:9]([F:17])([F:18])[C:10]1[CH:11]=[C:12]([I:1])[C:13]([OH:16])=[CH:14][CH:15]=1

Participants

7

Procedure

a,a a-Trifluoro-o-iodo-p-cresol. A mixture of iodine (91.6 mmol, 23.2 g) and sodium bicarbonate (91.6 mmol, 7.7 g) was added to a solution of α,α,α-trifluoro-p-cresol (83.3 mmol, 13.5 g) in THF (90 mL) and H2O (90 mL) and the reaction mixture was allowed to stand at room temperature overnight. Sufficient thiourea (5% solution) was added to remove the excess iodine as indicated by the color change of the reaction from deep violet to brown. The reaction mixture was extracted with ether (3×100 mL), the extract was dried, filtered and the filtrate was concentrated to obtain a brown oil. This oil was distilled (bp 105° C. at 44 mm Hg) to obtain α,α,α-trifluoro-o-iodo-p-cresol (4.1 g, 75% pure, admixed with the starting α,α,α-trifluoro-p-cresol).

Workup

  1. customto remove the excess iodine
  2. customas indicated by the color change of the reaction from deep violet to brown
  3. extractionThe reaction mixture was extracted with ether (3×100 mL)
  4. customthe extract was dried
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. customto obtain a brown oil
  8. distillationThis oil was distilled (bp 105° C. at 44 mm Hg)

Sources & evidence

ORD record
ord-61861ac0b05d4d949fccd3577cb0847f
Source dataset
uspto-grants-2003_06
Patent number
US06579879B2

Reaction notes

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