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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401349Generated: November 1, 2026

Pyridine → HCID 12458458, compound

https://huagongshe.com/reaction/2401349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant(E)-Acetaldehyde oximeHCID 5324279—
ReactantHCID 6999769HCID 6999769—
SolventChloroformHCID 6212—
ProductHCID 12458458HCID 12458458—

Reaction Steps

To a suspension of N-chlorosuccimide (71.5 g, 535 mmol) in CHCl3 (360 mL) and pyridine (1.61 g, 20.3 mmol) was added a solution of (E)-acetaldehyde oxime (31.6 g, 535 mmol). After a period of 1 h, propargylacetate (35.0 g, 357 mmol) in a minimum of CHCl3 was added to the previous mixture. Triethylamine (114 g, 1124 mmol) was then added dropwise and the reaction mixture was cooled in a water bath in order to maintain the internal temperature below the boiling point. After a period of 1 h, the reaction mixture was concentrated in vacuo followed by the addition of EtOAc. The mixture was filtered on a glass filter and the solid washed with EtOAc, the combined filtrates were evaporated. After evaporation, additional EtOAc was added and the previous process repeated. The EtOAc was evaporated and the crude product was purified on a on Biotage system (isocratic elution 40% EtOAc:60% Hexanes) and the fractions followed by LC/MS to provide the titled compound as a clear oil. LC/MS m/z 156 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796261B2
Source datasetuspto-grants-2014_08
ORD IDord-619851051efa43d6bad1c85bae07f348
Source noteuspto-grants-2014_08