HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 1-(4-Trimethylsilylethynyl-phenyl)-2,2-dimethylpropan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1-(4-Bromophenyl)-2,2-dimethylpropan-1-one | HCID 12812080 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | 1-(4-Trimethylsilylethynyl-phenyl)-2,2-dimethylpropan-1-one | HCID 20236863 | — |
Reaction Steps
1.4 g Bis-(triphenylphosphine)-palladium dichloride and 0.19 g CuI are added, at room temperature, to a solution of 10.5 g trimethylsilylacetylene and 23.6 g 1-(4-bromophenyl)-2,2-dimethylpropan-1-one in 350 ml absolute diethylamine. The reaction mixture is stirred during 20 hours at room temperature, evaporated to dryness at the rotary evaporator and the residue extracted several times with toluene. The toluene is evaporated off and the remaining tacky oil chromatographed on a silica-gel column with hexane/toluene 2:1 as mobile phase to give 1-(4-trimethylsilylethynyl-phenyl)-2,2-dimethylpropan-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04609668 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-d777a7d27d1e436e82168eafc3bd86d5 |
| Source note | uspto-grants-1986_09 |