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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126706Generated: October 30, 2026

Propargyl bromide → HCID 20541535, compound

https://huagongshe.com/reaction/126706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantMagnesiumHCID 5462224—
ReactantHCID 20541536HCID 20541536—
SolventDiethyl EtherHCID 3283—
ProductHCID 20541535HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254036
Source datasetuspto-grants-1981_03
ORD IDord-fcccf0fdc33543639a2bfb9d275a1f71
Source noteuspto-grants-1981_03