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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195577Generated: October 26, 2026

Tetrahydrofuran → 1,2-Phenanthrenedione

https://huagongshe.com/reaction/2195577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant9,10-Bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthreneHCID 68551787—
SolventEthanolHCID 702—
Product1,2-PhenanthrenedioneHCID 308056676%

Reaction Steps

Into a 20 mL volume eggplant-shaped flask, 80 mg of the above-prepared 9,10-bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthrene dimer, 10 mL of tetrahydrofuran, 43 mg of ethanol, and 0.4 mL of tetrabutylammonium fluoride were added and stirred at room temperature in air. The resultant reaction mixture was allowed to stand. Thereafter, the precipitate was collected by filtration and washed, thereby to give 28 mg of a phenanthrenequinone compound represented by the following chemical structural formula (1b-1) (hereinafter referred to as a “phenanthrenequinone compound (1b-1)”) (yield 76%) as a reddish brown-colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338027B2
Source datasetuspto-grants-2012_12
ORD IDord-9ca737a9f5214428ab90c08d96b3b452
Source noteuspto-grants-2012_12