HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258212Generated: October 26, 2026
tert-Butanol → Phenol, 2-(1,1-dimethylethyl)-4-(1,1,3,3-tetramethylbutyl)-
https://huagongshe.com/reaction/258212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 4-Tert-octylphenol | HCID 8814 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Phenol, 2-(1,1-dimethylethyl)-4-(1,1,3,3-tetramethylbutyl)- | HCID 605573 | 54% |
Reaction Steps
4-t-octylphenol (160 g, 0.78 mole) was dissolved in 400 ml anhydrous TFA. T-butyl alcohol (94.3 g, 1.27 mole) was added with stirring. The mixture was stoppered and stirred for 24 hours at ambient (~22° C.) temperature. This solution was diluted with 600 ml water, and the resulting upper organic layer was isolated in a separatory funnel. The crude product, 2-t-butyl-4-t-octylphenol, was dried over anhydrous magnesium sulfate and purified by eluting 35 g of the mixture with 70:30 hexanes:dichloromethane (v/v) in a 5×20 cm silica column, then eluted with 300 to 700 ml of solvent and collected in aliquots of 50 ml. Aliquots showing a single spot by TLC on silica eluted with 70:30 hexanes:dichloromethane (v/v) were combined and rotoevaporated to a thick syrup for a yield of 54%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05266283 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-843e434730ac4e9cbf0db26c285ece4a |
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| Source note | uspto-grants-1993_11 |
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