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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500290Generated: November 1, 2026

N-Fluorobenzenesulfonimide → HCID 90074665, compound

https://huagongshe.com/reaction/1500290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 67997695HCID 67997695—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90074665HCID 9007466545.7%

Reaction Steps

Lithium bis(trimethylsilyl)amide (0.45 mL, 1M in tetrahydrofuran, 0.45 mmol) is added to a solution of commercially available 5-bromo-2-(methylsulfonylmethyl)pyridine (102 mg, 0.408 mmol) in tetrahydrofuran (5 mL) at −78° C. After 45 minutes N-Fluorodibenzenesulfonamide (156 mg) in tetrahydrofuran (10 mL) is added to the reaction mixture at −78° C. over 5 minutes. After stirring for 20 minutes the reaction is quenched with water (10 mL) and ethyl acetate(10 mL). The reaction mixture is partitioned between saturated aqueous ammonium chloride solution (10 mL) and ethyl acetate (10 mL). The combined organic layers are washed with brine and concentrated to give the crude product, which is purified by flash column chromatography eluting from neat hexane to neat ethyl acetate to give the title compound (50 mg): m/z (Cl) 268 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206126B2
Source datasetuspto-grants-2015_12
ORD IDord-e87dcc581d9c466191d62b576098a0f9
Source noteuspto-grants-2015_12