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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450645Generated: November 1, 2026

Triethylamine → HCID 19976954, compound

https://huagongshe.com/reaction/1450645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
Reactant1-Pentyn-3-olHCID 92981—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
ProductHCID 19976954HCID 19976954—

Reaction Steps

Dissolved in 50 ml of chloroform were 5.0 g (57.5 mmol) of n-butylaldoxime and 0.3 ml of pyridine, to which 7.6 g (57.1 mmol) of N-chlorosuccinimide were added in small portions while the internal temperature was controlled not to exceed 35° C. After the addition, the resultant mixture was stirred at room temperature for 1 hour. To the solution, 6.0 g (71.4 mmol) of 1-pentyn-3-ol and 5.9 g (58.4 mmol) of triethylamine were added. The stirring was continued for 2 hours at 40°-50° C. After the solvent was distilled off under reduced pressure, water was added and the reaction product was then extracted with diethyl ether. After concentration, the residue was purified by silica gel chromatography (eluent: chloroform) so that 3-propyl-5-(1-hydroxypropyl)isoxazole was obtained. It was dissolved in acetone, oxidized with Jones' reagent under ice cooling, and purified by silica gel chromatography (eluent: chloroform), so that 3-propyl-5-propionylisoxazole was obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602160
Source datasetuspto-grants-1997_02
ORD IDord-283da8893718441db20fa02db110c14b
Source noteuspto-grants-1997_02