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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192948Generated: October 31, 2026

N-Fluorobenzenesulfonimide → HCID 59739620, compound

https://huagongshe.com/reaction/1192948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 59739546HCID 59739546—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59739620HCID 5973962098%

Reaction Steps

Phosphazene base 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2-lambda5-5,4-lambda5-5-catenadi(phosphazene) (P2-tBu) (2M in THF) (0.38 ml, 0.77 mmol) was added dropwise to a solution of 3-[chloro-(2,6-difluoro-phenyl)-methanesulfonyl]-5,5-dimethyl-4,5-dihydroisoxazole (0.2 g, 0.64 mmol) in THF (2 ml), and the solution was stirred for 10 minutes at room temperature. N-Fluorobenzenesulfonimide (NFSI) (0.15 g, 0.77 mmol) was added and the mixture was stirred for 1 hour. The reaction was quenched by addition of aqueous hydrochloric acid (2M). The mixture was diluted with ethyl acetate and the two phases were separated. The organic phase was washed several times with brine, dried over magnesium sulfate and concentrated. The crude product was purified by chromatography on silica gel (eluent: ethyl acetate/hexane) to give the product (Compound No. 1.21 of Table 27) as a white solid (44 mg, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680290B2
Source datasetuspto-grants-2014_03
ORD IDord-738319fc9d264ccabd4fafd244a84aef
Source noteuspto-grants-2014_03