HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500290Generated: November 1, 2026
N-Fluorobenzenesulfonimide → HCID 90074665, compound
https://huagongshe.com/reaction/1500290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 67997695 | HCID 67997695 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90074665 | HCID 90074665 | 45.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206126B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e87dcc581d9c466191d62b576098a0f9 |
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| Source note | uspto-grants-2015_12 |
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