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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361977Generated: October 25, 2026

Toluene → 4-(2-Hydroxy-4,5-dimethylbenzyl)-2,5-dimethylphenol

https://huagongshe.com/reaction/361977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-DimethylphenolHCID 7249—
Reactant4-Hydroxymethyl-2,5-dimethylphenolHCID 10942640—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(2-Hydroxy-4,5-dimethylbenzyl)-2,5-dimethylphenolHCID 5405659868.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

Into a 1 liter of four-necked flask were charged 1.90 g of para-toluene sulfonic acid, 24.43 g of 3,4-xylenol and 48.87 g of toluene. Further, keeping the temperature at 30° C., 7.61 g of 4-hydroxymethyl-2,5-dimethylphenol 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, 50 g of toluene and 50 g of ethyl acetate was added. Thereafter, 50 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 50 g of 1% aqueous oxalic acid solution, followed by stirring the mixture and by carrying out a phase separation. Thereafter, washing with 50 g of deionized water was repeated four times, and the oil phase was concentrated. To the concentrated mass, 100 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 50 g of ethyl acetate. After adding 200 g of toluene thereto,the resulting mixture was concentrated. To the concentrated mass, 100 g of toluene was added and the resulting mass was cooled to 20° C. and filtered. The filter cake was rinsed with 100 g of toluene and dried a whole day and night under reduced pressure at 45 ° C. to obtain 8.82 g of 4-(2-hydroxy-4,5-dimethylbenzyl)-2,5-dimethylphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866724
Source datasetuspto-grants-1999_02
ORD IDord-51765a1d10a84f428d5236e02478bee7
Source noteuspto-grants-1999_02