HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968000Generated: October 30, 2026
N-Fluorobenzenesulfonimide → HCID 21912186, compound
https://huagongshe.com/reaction/968000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | HCID 21912379 | HCID 21912379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21912186 | HCID 21912186 | — |
Reaction Steps
To a solution of [2-(4-bromo-2,6-dimethyl-phenoxy)-3,6-dimethyl-pyridin-4-yl]-(1-ethyl-propyl)-amine in dry THF was added n-butylitium at −78° C. After stirring at −78° C. for 10 min, (PhSO2)2NF was added and the resulting mixture was stirred at −78° C. for 30 min, the dry-ice bath was removed. After stirring for 5 min, the mixture was quenched with brine and extracted with ethyl acetate. The organic layer was separated, dried, and concentrated to dryness. The residue was purified through silica gel chromatography to give the title compound. 1H NMR(CDCl3) d 6.77(s, 1H), 6.73(s, 1H), 6.08(s, 1H), 3.3(m, 1H), 2.12(s, 3H), 2.09(s, 6H), 2.08(s, 3H), 1.4-1.8(m, 4H), 0.97(t, 6H), ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06956047B1 |
|---|
| Source dataset | uspto-grants-2005_10 |
|---|
| ORD ID | ord-8e81ff2510eb4b35bedb8530e3087bb4 |
|---|
| Source note | uspto-grants-2005_10 |
|---|