HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → HCID 13279245, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15585339 | HCID 15585339 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13279245 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657579 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-71ea017638fc4256834973164e506f99 |
| Source note | uspto-grants-1987_04 |