HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850399Generated: November 1, 2026
Trifluoromethanesulfonic acid → HCID 66760033, compound
https://huagongshe.com/reaction/1850399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 3,5-Xylenol, 2-methoxy- | HCID 6451446 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 66760033 | HCID 66760033 | 202.3% |
Reaction Steps
Further, by using 2-methoxy-3,5-dimethylphenol (7.60 g, 41.7 mmol), synthesis was also performed according to the following method. That is, to a solution of n-heptane (76 mL) containing 2-methoxy-3,5-dimethylphenol (7.60 g, 41.7 mmol) and isobutyl aldehyde (5.71 mL, 62.6 mmol), trifluoromethanesulfonic acid (1.85 mL, 20.9 mmol) was added dropwise, and the mixture was stirred at 55° C. for 2.5 hours. After cooled to room temperature, the reaction solution was washed with water and dried using anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by basic silica gel chromatography (hexane-ethyl acetate 100:0) and silica gel chromatography (hexane-ethyl acetate 100:0-95:5) to give 8.70 g of the title compound (yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957069B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f701e01ed7074302b2dd7aaf0f68e0ba |
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| Source note | uspto-grants-2015_02 |
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