HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413570Generated: November 3, 2026
Propargyl bromide → 4-Trimethylsilylethynyl-1-octyn-4-ol
https://huagongshe.com/reaction/1413570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Heptyn-3-one, 1-(trimethylsilyl)- | HCID 11019511 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Trimethylsilylethynyl-1-octyn-4-ol | HCID 12786193 | — |
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 stirred mixture is cooled in an ice-water bath and a solution of 9.64 grams of n-butyl trimethylsilylethynyl ketone and 3.51 ml of propargyl bromide in 13 ml of ether added dropwise so that the mixture is very gently boiling 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 liquor is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is evaporated to dryness giving 10.5 grams of a red liquid. The liquid is Kugelrohr-distilled at 60° C./0.25-0.3 mm. The pale yellow liquid distillate which is the desired product weighed 8.5 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04250325 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-ed7d8ee6fe104aa3beedd5453cdff17e |
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| Source note | uspto-grants-1981_02 |
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