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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495756Generated: October 29, 2026

Benzophenone → 3,6,6-Triphenylfulvene

https://huagongshe.com/reaction/495756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantHexaneHCID 8058—
ReactantPhenylcyclopentadieneHCID 244167—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product3,6,6-TriphenylfulveneHCID 22327814—

Reaction Steps

A solution of 2.5 g (17.6 mmol) of phenylcyclopentadiene in 30 ml of toluene was ice cooled, and thereto was dropwise added 13.0 ml (21.1 mmol) of a hexane solution of n-butyllithium. The resulting white slurry was stirred at room temperature for one night. From the slurry, the solvent was filtered off to give a THF solution (brown solution). To the solution, a solution of 3.2 g (17.6 mmol) of benzophenone in 10 ml of THF was added, followed by stirring at room temperature for one night. After addition of water, the mixture was subjected to extraction with diethyl ether and dried over magnesium sulfate. Then, the ether was distilled off to obtain a red viscous liquid. The liquid was purified by a silica gel column to obtain a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939928B1
Source datasetuspto-grants-2005_09
ORD IDord-e825ebb655e14025b027e8f794278c2b
Source noteuspto-grants-2005_09