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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656805Generated: November 2, 2026

N-Fluorobenzenesulfonimide → 1-Fluoroanthracene

https://huagongshe.com/reaction/1656805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
Reactant1-BromoanthraceneHCID 12529827—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-FluoroanthraceneHCID 1306865576%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.2 millimoles n-butyl lithium were dropped into a solution of 1 millimole bromoanthracene in 5 milliliters diethyl ether at 5° C. The solution was cooled to 0° C, was stirred for 1 hour, and then was cooled further to -78° C.; 1.2 millimoles N-fluorobenzenesulfonimide prepared according to Example 1 above in 5 milliliters tetrahydrofuran were dropped into the mixture which was stirred for 1 hour. The temperature was allowed to rise to 20° C. while stirring was continued. The reaction mixture was quenched by pouring into saturated ammonium chloride solution and extracted with diethyl ether. Fluoroanthracene was obtained in 76% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254732
Source datasetuspto-grants-1993_10
ORD IDord-0976ee40ade44b278d4c711e160891a9
Source noteuspto-grants-1993_10