Iodine → 4-Chloro-2-iodophenol

HRID 22742

Reaction equation

HRID 22742 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.O.[I:10]I.C(=O)(O)[O-].[Na+]>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([I:10])[CH:3]=1

Participants

6

Procedure

To a solution of 4-chlorophenol in THF (75 mL), and H2O (75 mL) was added a mixture of crushed iodine (78.7 mmol, 20 g) and sodium bicarbonate (78.7 mmol, 6.6 g). The reaction mixture was stirred at room temperature overnight, then quenched with sufficient 5% sodium thiosulfate solution to turn the color of the reaction mixture from deep violet to light yellow and extracted with ether (2×200 mL). The ether layer was collected, washed with H2O, and the washed ether layer was dried, filtered and the filtrate was evaporated to a crude product, which was purified by distillation to obtain 4-chloro-2-iodo phenol (7%, 1.3 g); mp 79° C.-82° C.

Workup

  1. customquenched with sufficient 5% sodium thiosulfate solution
  2. extractionextracted with ether (2×200 mL)
  3. customThe ether layer was collected
  4. washwashed with H2O
  5. dry with materialthe washed ether layer was dried
  6. filtrationfiltered
  7. customthe filtrate was evaporated to a crude product, which
  8. distillationwas purified by distillation

Sources & evidence

ORD record
ord-377ea90ca4ef427b88176d5de2f9524e
Source dataset
uspto-grants-2005_02
Patent number
US06849629B2

Linked notes

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