HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466513Generated: October 29, 2026
Trimethylsilylacetylene → HCID 15021947, compound
https://huagongshe.com/reaction/466513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4-Ethyl-1-(4-iodophenyl)-2,6,7-trioxabicyclo[2,2,2]octane | HCID 15021946 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | HCID 15021947 | HCID 15021947 | — |
Reaction Steps
Bis-triphenylphosphine palladium dichloride (60 mg) and cuprous iodide (10 mg) were added to a stirred solution of 4-ethyl-1-(4-iodophenyl)-2,6,7-trioxabicyclo[2,2,2]octane (1.5 gms) and trimethylsilylacetylene (0.92 ml) in dry diethylamine (40 ml) under nitrogen. The resulting mixture was stirred at room temperature for 16 hours. After this time the solvent was removed under vacuum and the residue extracted with diethylether. 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, eluting with 30% dichloromethane in hexane saturated with ammonia. 4-Ethyl-1-[4-(2-trimethylsilylethynyl)-phenyl]-2,6,7-trioxabicyclo[2,2,2]octane (1.2 gms) was obtained as an off-white solid (1.2 gms) after recrystallisation from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157029 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-54da0ad793dd4e11969a6e84bb943a7e |
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| Source note | uspto-grants-1992_10 |
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