HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → Methyl 2-chloro-5-((trimethylsilyl)ethynyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Methyl 2-chloro-5-iodobenzoate | HCID 35563912 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418903 | HCID 178418903 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 2-chloro-5-((trimethylsilyl)ethynyl)benzoate | HCID 57422929 | 98.1% |
Reaction Steps
A mixture of 2-chloro-5-iodo-benzoic acid methyl ester (3.5 g, 12 mmol), dichlorobis(triphenylphosphino)palladium(II) (0.04 g, 0.06 mmol), triphenylphosphine (0.06 g, 0.24 mmol), copper iodide (0.05 g, 0.24 mmol), (trimethylsilyl)acetylene (1.9 g, 19.2 mmol) in triethylamine (40 mL) was heated at reflux for 12 h. The mixture was concentrated in vacuo, diluted with ethyl acetate (150 mL) and washed sequentially with 10% aqueous citric acid, water, and brine. The organic solution was dried, filtered and concentrated in vacuo to afford the title compound (3.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186742B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-35f1d8e447844d7bb99c7c89a2e4d1d5 |
| Source note | uspto-grants-2007_03 |