Water → 4-[(4-Hydroxy-3-methylphenyl)methyl]-2,5-dimethylphenol

HRID 361975Notes

Reaction equation

HRID 361975 reaction equation
[C:1]1([CH3:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O:11][CH2:12][CH3:13])(=O)C.[OH2:14]>>[OH:14][C:2]1[CH:3]=[CH:4][C:5]([CH2:7][C:1]2[C:6]([CH3:5])=[CH:13][C:12]([OH:11])=[C:3]([CH3:4])[CH:2]=2)=[CH:6][C:1]=1[CH3:7]

Participants

4

Conditions

Temperature
20 °C

Procedure

Into a 1 liter of four-necked flask were charged 4.76 g of para-toluenesulfonic acid, 54.07 g of ortho-cresol and 108.14 g of methanol. Further, keeping the temperature at 30° C., 38.05 g of 4-hydroxymethyl-2,5-dimethylphenol obtained above was added in ten portions over 1 hour. The mixture was stirred at the same temperature for 2 more hours. After completion of the reaction, 200 g of toluene and 200 gof ethyl acetate was added. Thereafter, 200 g of deionized water was added and the resulting mixture was stirred and a phase separation was carried out. Then, metal content was removed by adding 200 g of 1% aqueous oxalic acid solution, followed by stirring the mixture and by carrying out a phase separation. Thereafter, washing with 200 g of deionized water was repeated four times, and the oil phase was concentrated. To the concentrated mass, 200 g of toluene was added and the resulting solution was cooled to 20° C. and filtered. The filter cake was rinsed with 200 g of toluene and dissolved in 200 g of ethyl acetate. After adding 200g of toluene thereto, the resulting mixture was concentrated. To the concentrated mass, 200 g of toluene was added and the resulting mass was cooled to 20° C. and filtered. The filter cake was rinsed with 200 g of toluene and dried a whole day and night under reduced pressure at 45° C. to obtain 20.12 g of 4-(4-hydroxy-3-methylbenzyl)-2,5-dimethylphenol.

Workup

  1. additionabove was added in ten portions over 1 hour
  2. additionwas added
  3. stirringthe resulting mixture was stirred
  4. customa phase separation
  5. customThen, metal content was removed
  6. additionby adding 200 g of 1% aqueous oxalic acid solution
  7. stirringby stirring the mixture
  8. customa phase separation
  9. washThereafter, washing with 200 g of deionized water
  10. concentrationthe oil phase was concentrated
  11. additionTo the concentrated mass, 200 g of toluene was added
  12. filtrationfiltered
  13. washThe filter cake was rinsed with 200 g of toluene
  14. dissolutiondissolved in 200 g of ethyl acetate
  15. additionAfter adding 200g of toluene
  16. concentrationthe resulting mixture was concentrated
  17. additionTo the concentrated mass, 200 g of toluene was added
  18. temperaturethe resulting mass was cooled to 20° C.
  19. filtrationfiltered
  20. washThe filter cake was rinsed with 200 g of toluene
  21. customdried a whole day and night under reduced pressure at 45° C.

Sources & evidence

ORD record
ord-52e4616b62134c6bb77c5aa1c478292e
Source dataset
uspto-grants-1999_02
Patent number
US05866724

Reaction notes

Loading…