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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596544Generated: October 25, 2026

Fluorene-2-carboxaldehyde → 2-ethenyl-9H-fluorene

https://huagongshe.com/reaction/596544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluorene-2-carboxaldehydeHCID 34804—
ReactantTriphenylmethyl phosphonium bromideHCID 21951224—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-ethenyl-9H-fluoreneHCID 11041607—

Reaction Steps

Triphenylmethyl phosphonium bromide (36 gms/0.1 mole) in 500 milliliters of dry THF is treated under nitrogen with 90 milliliters of a 1.1 molar solution of n-butyl lithium in hexane and stirred for 2 hours. A solution of 19.4 gms. (0.1 mole) of fluorene-2-carboxaldehyde in 100 milliliters of THF is added dropwise and the final mixture refluxed for 11/2 hours. One liter of hexane is added to the cold solution and the precipitate filtered off. The filtrate is evaporated and the residue chromatographed on alumina (Woehlm neutral) using hexane to give 15 gms. (75% theory) of product. Recrystallization from hexane yields 2-vinylfluorene as colorless plates. The structure of the product is confirmed by nuclear magnetic resonance and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011266
Source datasetuspto-grants-1977_03
ORD IDord-0da5f13a5e9a40c78ab8d905c83a7eb5
Source noteuspto-grants-1977_03