HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → [2-(3,5-Dichlorophenyl)ethynyl]trimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1,3-Dichloro-5-iodobenzene | HCID 76424 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | [2-(3,5-Dichlorophenyl)ethynyl]trimethylsilane | HCID 22570337 | — |
Reaction Steps
To a solution of 1,3-dichloro-5-iodo-benzene (5.44 g, 20 mmol) in diethylamine (75 mL) was added PdCl2(PPh3)2 (280 mg, 0.4 mmol), trimethylsilylacetylene (2.36 g, 24.0 mmol) and copper(I)iodide (20 mg, 0.1 mmol). The reaction mixture was stirred at room temperature for 24 h, filtered and evaporated. The residue was purified by column chromatography using heptane:ethyl acetate (8:2) as eluent. The desired (3,5-dichloro-phenylethynyl)-trimethylsilane product was isolated in 4.85 g yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06569901B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-061369dd3e2d4ce58ce9ce7d9fca3fbb |
| Source note | uspto-grants-2003_05 |