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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant4-Tert-butyl-5-hydroxy-2-octylbenzofuranHCID 23442864—
Product4-Tert-butyl-5-hydroxy-2-octyl-2,3-dihydrobenzofuranHCID 2344288683%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663373
Source datasetuspto-grants-1997_09
ORD IDord-b74942d0113143dea14ee564c582614f
Source noteuspto-grants-1997_09