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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126724Generated: October 26, 2026

Propargyl bromide → 4-Trimethylsilylethynyl-1-octyn-4-ol

https://huagongshe.com/reaction/126724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantMagnesiumHCID 5462224—
Reactant1-Heptyn-3-one, 1-(trimethylsilyl)-HCID 11019511—
SolventDiethyl EtherHCID 3283—
Product4-Trimethylsilylethynyl-1-octyn-4-olHCID 12786193—

Reaction Steps

To a stirred suspension of 1.29 g. 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 stirred mixture is cooled in an ice-water bath and a solution of 9.64 g. of n-butyl trimethylsilylethynyl ketone and 3.51 ml. of propargyl bromide in 13 ml. of ether is added, dropwise so that the mixture is very gently boiling during 40 minutes. After addition, the cooling bath is removed and the mixture is stirred at room temperature for 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 liquor is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is evaporated to dryness giving 10.5 g. of a red liquid. This liquid is Kugelrohr-distilled at 60° C./0.25-0.3 mm. The pale yellow liquid distillage which is the desired product weighs 8.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254036
Source datasetuspto-grants-1981_03
ORD IDord-031aef73628548ba8568335c77e63bc9
Source noteuspto-grants-1981_03