HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126706Generated: October 30, 2026
Propargyl bromide → HCID 20541535, compound
https://huagongshe.com/reaction/126706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 20541536 | HCID 20541536 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20541535 | HCID 20541535 | — |
Reaction Steps
To a stirred suspension of 1.29 grams of magnesium and 10 mg. of mercuric chloride in 12 ml. of ether is added 0.4 ml. of propargyl bromide. The reaction is initiated after stirring at room temperature for a few minutes. The solution of 11.2 grams of 3-chloropropyl trimethylsilylethynyl ketone and 3.51 ml. of propargyl bromide in 13 ml. of ether is added dropwise so that the mixture is very gently boiled during a period of about 40 minutes. After addition is complete, the cooling bath is removed and the mixture is stirred at room temperature for about 1.5 hours. The mixture is recooled in an ice bath and 10 ml. of saturated ammonium chloride solution is added. The resulting white mixture is filtered through diatomaceous earth. The clear mother liquid is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is evaporated to dryness giving a red liquid. The liquid is Kugelrohr-distilled to afford the pale yellow liquid distillate which is the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04254036 |
|---|
| Source dataset | uspto-grants-1981_03 |
|---|
| ORD ID | ord-fcccf0fdc33543639a2bfb9d275a1f71 |
|---|
| Source note | uspto-grants-1981_03 |
|---|