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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896679Generated: October 31, 2026

N-Fluorobenzenesulfonimide → HCID 10189127, compound

https://huagongshe.com/reaction/896679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 9960211HCID 9960211—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 10189127HCID 10189127—

Reaction Conditions

Temperature21 °C

Reaction Steps

To a solution of Example 1 (200 mg, 0.34 mmol) in THF/DMF (1:1, 10 mL) at 0° C. was added potassium tert-butoxide (1M, THF, 0.34 mL, 0.34 mmol) dropwise. After 15 min, N-fluorobenzene sulfonimide (212 mg, 0.73 mmol) was added and the reaction mixture stirred for 2 h at 21° C. The resulting mixture was diluted with a saturated ammonium chloride solution and ethyl acetate. The organic extracts were washed (H2O), (brine), dried (MgSO4), filtered and concentrated. Purification by flash chromatography (eluting with toluene/acetone, 80:20) provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919353B2
Source datasetuspto-grants-2005_07
ORD IDord-3c2288d729d4483282c3ec3537a06fe4
Source noteuspto-grants-2005_07