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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488236Generated: October 26, 2026

Phenyl Trifluoromethanesulfonate → 2-Triethylsilyl-5-phenyl-4-furaldehyde

https://huagongshe.com/reaction/488236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl TrifluoromethanesulfonateHCID 548641—
Reactant3-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 10878438—
ReactantHCID 178506926HCID 178506926—
CatalystZincchlorideHCID 3007855—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Product2-Triethylsilyl-5-phenyl-4-furaldehydeHCID 19433144—

Reaction Steps

Treatment of 2-triethylsilyl-4-furaldehyde with lithio N,N,N'-trimethylethylenediamine, followed by phenyl trifluoromethanesulfonate in the presence of anhydrous zinc chloride and tetrakis (triphenylphosphine) palladium (o) and work up gives the titled aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298633
Source datasetuspto-grants-1994_03
ORD IDord-018130448c9e46a38cdbaf860961e47e
Source noteuspto-grants-1994_03