HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 18383984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Octyne | HCID 12370 | — |
| Reactant | Benzaldehyde, 3-iodo-4-(methoxymethoxy)- | HCID 10402059 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18383984 | HCID 18383984 | 45.2% |
Reaction Steps
Under an argon atmosphere, copper iodide (190 mg, 1.0 mmol), 1-octyne (0.55 mL, 5.0 mmol) and 3-iodo-4-methoxymethoxybenzaldehyde (291 mg, 1.0 mmol) were added to a solution (2 mL) of palladium (II) diacetate (11 mg, 0.05 mmol) and triphenylphosphine (52 mg, 0.20 mmol) in methylene chloride, followed by stirring at room temperature for 2 hours. Next, the reaction solution was filtered through celite, and the solvent contained in the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluted with ethyl acetate/hexane=1/10) to give 3-(1-octyn-1-yl)-4-methoxymethoxybenzaldehyde (124 mg, yield 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492392B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-b2f9cf1afa254210951bad91ae577cd5 |
| Source note | uspto-grants-2002_12 |