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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059655Generated: November 1, 2026

N-Fluorobenzenesulfonimide → HCID 22175082, compound

https://huagongshe.com/reaction/1059655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 15635484HCID 15635484—
ReactantAcetone hexaneHCID 21880519—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22175082HCID 2217508256%

Reaction Steps

To a stirred solution of 9 (12.39 g, 0.055 mol) in ether (200 mL) cooled to ≦−70° C. under an atmosphere of argon was slowly added t-BuLi (40 mL, 1.5 M pentane solution). During the addition, the reaction temperature was maintained at ≦−68° C. After the addition was complete the mixture was stirred an additional 60 minutes at ≦−70° C., then transferred via cannula to a stirred solution of N-fluorobenzenesulfonimide (18.92 g) in dry THF (200 mL) which was also cooled to ≦−70° C. under argon. After the addition was complete, the cooling bath was removed and the reaction mixture was allowed to warm up to room temperature. Water (100 mL) was added and the organic phase was separated, dried (MgSO4) and concentrated to give a brown oil. Chromatography (silica gel, hexane-acetone, 9:1) gave the desired product 10 as an orange oil (7.5 g) which contained about 15% starting material. This crude mixture was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521622B1
Source datasetuspto-grants-2003_02
ORD IDord-b8cea4e9fbb44a9db3fbf04e25647301
Source noteuspto-grants-2003_02