HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 22504370, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Ethyl 5-bromofuran-2-carboxylate | HCID 345282 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22504370 | HCID 22504370 | — |
Reaction Steps
A solution of 5 g of the product of Stage A, 15 ml of acetonitrile, 15 ml of triethylamine, 4.5 ml of ethynyltrimethylsilane, 170 mg of (triphenylphosphine)palladium chloride and 30 mg of copper iodide was heated at 40° C. for 2 and a half hours and then allowed to return to room temperature and was poured into an aqueous sodium dihydrogenphosphate solution. The mixture was extracted with ethyl acetate and the extract was washed with water and dried. The solvent was evaporated to obtain after chromatography on silica (eluent: 95/5 hexane/ethyl acetate) 4.75 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405865 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-9c9e74152e1d4572aa7f5f20a5e36702 |
| Source note | uspto-grants-1995_04 |