HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223662Generated: October 30, 2026
Propargyl bromide → HCID 178459972, compound
https://huagongshe.com/reaction/223662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178526276 | HCID 178526276 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178459972 | HCID 178459972 | — |
Reaction Steps
1.31 g. of sodium hydride (55% strength suspension) are added to a solution of 6.15 g. of 2-[(2,6-dichlorophenyl)imino]-1-hydroxyimidazolidine in 45 ml. of absolute dimethylformamide at a temperature of 25°. After 30 minutes, 4.16 g. of propargyl bromide are added dropwise. After 30 minutes, the mixture is poured onto 500 ml. of a saturated solution of sodium chloride and the aqueous phase is extracted with ether. The ether extracts are washed with aqueous hydrochloric acid. The aqueous extracts are then rendered basic with 3 N caustic soda solution and extracted with ether. After evaporating off the solvent, the residue is dissolved in ether, and hydrogen chloride in dioxane is added. The residue is recrystallized from methanol/acetonitrile, whereupon 2-[(2,6-dichlorophenyl)imino]-1-(2-propynyloxy)-imidazolidine hydrochloride, m.p. 198°-199° (from methanol/acetonitrile) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04355033 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-0652df65b9c7466b91db3963b5f72e3c |
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| Source note | uspto-grants-1982_10 |
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