HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224510Generated: October 27, 2026
1,2-Dibromoethane → HCID 20565008, compound
https://huagongshe.com/reaction/224510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methylenepentanal | HCID 70609 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20565008 | HCID 20565008 | — |
Reaction Steps
To a stirred mixture of 12.16 g. of magnesium in 120 ml. of ether containing 200 mg. of mercuric chloride is added 2 ml. of propargyl bromide and 0.5 ml. of 1,2-dibromoethane. This mixture is stirred under argon until the reaction begins. To this is added with stirring a solution of 41.57 g. of 2-methylene valeraldehyde and 64.95 g. of propargyl bromide in 90 ml. of ether, dropwise, at a rate to maintain reflux. After addition is complete the mixture is refluxed 15 minutes, stirred at room temperature one hour, cooled to 0° C. and saturated ammonium chloride solution is added dropwise until reflux stops. The mixture is filtered through Celite, dried over magnesium sulfate and the ether is removed giving the product as a light orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04232166 |
|---|
| Source dataset | uspto-grants-1980_11 |
|---|
| ORD ID | ord-2b50041a367a469da397523184c3a249 |
|---|
| Source note | uspto-grants-1980_11 |
|---|