HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260845Generated: October 30, 2026
N-Fluorobenzenesulfonimide → 1-Fluoroanthracene
https://huagongshe.com/reaction/2260845
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | 1-Bromoanthracene | HCID 12529827 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Fluoroanthracene | HCID 13068655 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478964 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-944d7f9977f641f8aa558b544aaeee0b |
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| Source note | uspto-grants-1995_12 |
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