HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → [(2,3-Dichlorophenyl)ethynyl](trimethyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1,2-Dichloro-3-iodobenzene | HCID 75459 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | [(2,3-Dichlorophenyl)ethynyl](trimethyl)silane | HCID 69198883 | — |
Reaction Steps
1,2-Dichloro-3-iodobenzene (4.95 g, 18.1 mmol), trimethylsilylacetylene (2 g, 20 mmol), bis(triphenylphosphine)palladium(II)chloride (245 mg, 0.35 mmol), and copper(I)iodide (45 mg, 0.24 mmol) were combined in triethylamine (120 mL) and heated at reflux for 45 minutes. The mixture was allowed to cool to room temperature and was then partitioned between diethyl ether and saturated sodium chloride. The organic phase was dried with sodium sulfate, filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was taken directly on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709469B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-7d7ee3507aef4eb1b1de0440e10cbfe9 |
| Source note | uspto-grants-2010_05 |