Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409645Generated: October 30, 2026

Pyridine → HCID 66685413, compound

https://huagongshe.com/reaction/409645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 86683903HCID 86683903—
SolventDichloromethaneHCID 6344—
ProductHCID 66685413HCID 66685413—

Reaction Steps

(E)-Methyl 2-((2-(hex-4-en-1-yloxy)-2-oxoethyl)amino)-2-oxoacetate (0.24 g, 1 eq) and DCM (2.4 mL) were added to a vessel with stirring followed by the addition of pyridine (95 mg, 1.2 eq). Tf2O (0.42 g, 1.5 eq) was then added over 45 min at ambient temperature and the mixture was stirred at ambient temperature for 48 h. The mixture was washed with 20 wt % aqueous NaOAc (2×1.5 mL), 10 wt % aqueous citric acid (3×1.5 mL), and water (1×1.5 mL). The organic layer was then concentrated under reduced pressure to provide the title compound as a solid. 1H NMR (300 MHz, CDCl3) δ ppm 8.10 (s, 1H), 4.15-4.25 (m, 2H), 3.94 (s, 3H), 2.71 (t, J=6.56 Hz, 2H), 2.47 (s, 3H), 2.00-2.18 (m, 2H); 13C NMR (75 MHz, CDCl3) δ ppm 166.71, 153.50, 138.69, 136.72, 135.67, 130.36, 65.93, 52.35, 22.18, 21.49, 14.57; HRMS (M+H) m/z, calcd for C11H14NO3, 208.0974; found 208.0981.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759523B2
Source datasetuspto-grants-2014_06
ORD IDord-da71c7dc5d0d42a8ab53f899e4ed2b87
Source noteuspto-grants-2014_06