Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968000Generated: October 30, 2026

N-Fluorobenzenesulfonimide → HCID 21912186, compound

https://huagongshe.com/reaction/968000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 21912379HCID 21912379—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21912186HCID 21912186—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956047B1
Source datasetuspto-grants-2005_10
ORD IDord-8e81ff2510eb4b35bedb8530e3087bb4
Source noteuspto-grants-2005_10