Hydrochloric Acid → 4-iodo-2-methoxyphenol

HRID 1532987Notes

Reaction equation

HRID 1532987 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.S([O-])([O-])=O.[Na+].[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, 7.2% 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 sulfite (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-9616f72f78e54859bf28459a527921b4
Source dataset
uspto-grants-2001_03
Patent number
US06207662B1

Reaction notes

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