Water → 4-[(4-Hydroxy-3-methylphenyl)methyl]-2,5-dimethylphenol
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
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
- additionabove was added in ten portions over 1 hour
- additionwas added
- stirringthe resulting mixture was stirred
- customa phase separation
- customThen, metal content was removed
- additionby adding 200 g of 1% aqueous oxalic acid solution
- stirringby stirring the mixture
- customa phase separation
- washThereafter, washing with 200 g of deionized water
- concentrationthe oil phase was concentrated
- additionTo the concentrated mass, 200 g of toluene was added
- filtrationfiltered
- washThe filter cake was rinsed with 200 g of toluene
- dissolutiondissolved in 200 g of ethyl acetate
- additionAfter adding 200g of toluene
- concentrationthe resulting mixture was concentrated
- additionTo the concentrated mass, 200 g of toluene was added
- temperaturethe resulting mass was cooled to 20° C.
- filtrationfiltered
- washThe filter cake was rinsed with 200 g of toluene
- 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
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