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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452345Generated: October 30, 2026

Trifluoroacetic acid → 2,4,6-Tri-tert-butyl-5-hydroxy-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/1452345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantSodium HydroxideHCID 14798—
Reactant2,4,6-Tri-tert-butyl-5-hydroxybenzofuranHCID 11822804—
Product2,4,6-Tri-tert-butyl-5-hydroxy-2,3-dihydrobenzofuranHCID 1107758476.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylsilane (76 ml) was added to 2,4,6-tri-tert-butyl-5-hydroxybenzofuran (24.7 g, 82 mmol) and trifluoroacetic acid (38 ml) was added dropwise to the mixture under ice cooling. The mixture was stirred first at 0° C. for 15 min, then at room temperature for 15 min before it was poured into ice water. The mixture was neutralized with an aqueous solution of 1N sodium hydroxide and subjected to extraction with ethyl acetate. The extracted 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 2,4,6-tri-tert-butyl-5-hydroxy-2,3-dihydrobenzofuran [19.0 g (yield, 76%)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-0552ca49df1943b387a199163d92bdb4
Source noteuspto-grants-1997_02