Hydrochloric Acid → 4-iodo-2-methoxyphenol

HRID 1017244Notes

Reaction equation

HRID 1017244 reaction equation
[C:1]1([O:8][CH3:9])[C:2](=[CH:4][CH:5]=[CH:6][CH:7]=1)[OH:3].[I-:10].[Na+].[OH-].[Na+].Cl[O-].[Na+].Cl.[Na]>CO>[I:10][C:6]1[CH:5]=[CH:4][C:2]([OH:3])=[C:1]([O:8][CH3:9])[CH:7]=1

Participants

8

Conditions

Temperature
0 °C

Procedure

4-Iodo-2-methoxyphenol was prepared according to the method described by K. J. Edgar and N. Falling, J. Org. Chem. 55, 5287 (1990). Guaiacol (50.0 g, 402 mmol), sodium iodide (60.5 g, 402 mmol) was dissolved in methanol (800 ml) and cooled to 0° C., and sodium hydroxide (16.0 g, 402 mmol) was added at such a rate that the temperature did not exceed 5° C. An aqueous solution of sodium hypochlorite (750 ml, 72% solution, 402 mmol) was added during 45 min. The temperature was not allowed to exceed 0° C. After completed addition it was stirred for another 10 minutes at 0° C. First aqueous hydrochloric acid (100 ml, 4 M solution) and then sodium sulifite (200 ml saturated aqueous solution) was added. The product was extracted with ether was followed by drying over magnesium sulfate. Evaporation of the solvent was followed by distillation and the fraction at 105-106° C. at 0.1 mm Hg was collected. Yield 55 g, 54%.

Workup

  1. customdid not exceed 5° C
  2. customto exceed 0° C
  3. additionaddition it
  4. extractionThe product was extracted with ether
  5. dry with materialby drying over magnesium sulfate
  6. customEvaporation of the solvent
  7. distillationwas followed by distillation
  8. customthe fraction at 105-106° C. at 0.1 mm Hg was collected

Sources & evidence

ORD record
ord-4a54b705b4604fc486fb9468e98b807d
Source dataset
uspto-grants-2002_11
Patent number
US06479491B1

Reaction notes

Loading…