HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345292Generated: October 31, 2026
Trimethylsilylacetylene → HCID 19992007, compound
https://huagongshe.com/reaction/345292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Pyridine, 2-iodo-5-(4-propyl-2,6,7-trioxabicyclo(2.2.2)oct-1-yl)- | HCID 3086954 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | HCID 19992007 | HCID 19992007 | — |
Reaction Steps
Bis-triphenylphosphine palladium dichloride (15 mg) and cuprous iodide (5 mg) were added to a stirred solution of 1-(6-iodo-3-pyridyl)-4-n-propyl-2,6,7-trioxabicyclo[2.2.2] octane (430 mg.) and trimethylsilyl acetylene (252 μl) in dry diethylamine (10 ml) under nitrogen. The resulting mixture was stirred at room temperature for 4 hours. The solvent was removed in vacuo and the residue extracted with diethyl ether. The ethereal solution was washed with water, dried over anhydrous magnesium sulphate and evaporated in vacuo. The residue was purified by column chromatography on alumina (Alumina Woelm TSC), eluting with 1:6 dichloromethane:hexane, saturated with ammonia. 4-n-Propyl-1-[6-(2-trimethylsilylethynyl)-3-pyridyl]-2,6,7-trioxabicyclo[2.2.2]octane (282 mg) was obtained as a pale brown crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057504 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-3a552aeff9ab4b4d90bae93b318d452d |
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| Source note | uspto-grants-1991_10 |
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