Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542382Generated: October 31, 2026

Propargyl bromide → HCID 13279245, compound

https://huagongshe.com/reaction/542382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15585339HCID 15585339—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13279245HCID 13279245—

Reaction Steps

A mixture of 5.0 g (0.025 mol) N-(4,6-dimethylpyrimidin-5-yl)-chloroacetamide and 1.0 g tetrabutylammoniumchloride in 150 ml CH2Cl2 and 6.0 g propargylbromide is cooled to 8°, and 15 ml 50% aqueous NaOH are added dropwise thereto, whereby the temperature gradually rises to 20°. The reaction temperature is maintained at 18° to 20° with cooling. The mixture is stirred during 21/2 hours and then diluted with 100 ml H2O. The organic phase is separated off and dried over Na2SO4. The dried solution is evaporated to give a brown powder that is chromatographed on silica gel with the aid of diethylether (Rf=0.15), yielding the title compound in the form of white crystals m.p. 122°-123°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04657579
Source datasetuspto-grants-1987_04
ORD IDord-71ea017638fc4256834973164e506f99
Source noteuspto-grants-1987_04