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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206677Generated: October 31, 2026

N-Fluorobenzenesulfonimide → HCID 118074105, compound

https://huagongshe.com/reaction/2206677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 86714019HCID 86714019—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118074105HCID 118074105—

Reaction Steps

To a solution of the intermediate 17 (1.01 g, 1.2 mmol) in anhydrous THF (12.0 mL) were added dropwise n-BuLi (2.5 M in hexane, 0.77 mL, 1.92 mmol) at −78° C. under nitrogen atmosphere, and the mixture was stirred for 20 min at the same temperature. Then a solution of N-fluorobenzenesulfonimide (0.68 g, 2.16 mmol) in THF (3.0 mL) was added dropwise, and the mixture was stirred for 1 h at the same temperature. The reaction mixture was quenched with saturated NaCl solution (10 mL) and extracted with EtOAc (50 mL). The organic layer was washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to provide the crude intermediate 19, which was used without further purification (0.95 g, 1.21 mmol, 101%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-ad2be5091f8f4338ad8855689059b788
Source noteuspto-grants-2016_06