HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376969Generated: October 30, 2026
Trifluoroacetic acid → 4-Tert-butyl-5-hydroxy-2-octyl-2,3-dihydrobenzofuran
https://huagongshe.com/reaction/1376969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4-Tert-butyl-5-hydroxy-2-octylbenzofuran | HCID 23442864 | — |
| Product | 4-Tert-butyl-5-hydroxy-2-octyl-2,3-dihydrobenzofuran | HCID 23442886 | 83% |
Reaction Steps
Triethylsilane (2.8 ml) was added to 4-tert-butyl-5-hydroxy-2-octylbenzofuran (300 mg, 1.0 mmol) and, then, trifluoroacetic acid (1.4 ml) was added dropwise under ice cooling. The mixture was stirred first at 0° C. for 15 min, then at room temperature for 1 h., Thereafter, the mixture was poured into ice water and subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (chloroform) to afford 4-tert-butyl-5-hydroxy-2-octyl-2,3-dihydrobenzofuran [252 mg (yield, 83%)] as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663373 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-b74942d0113143dea14ee564c582614f |
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| Source note | uspto-grants-1997_09 |
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