HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Dodecyne → 2-(1-Dodecyn-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Dodecyne | HCID 69821 | — |
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(1-Dodecyn-1-yl)benzaldehyde | HCID 19778789 | — |
Reaction Steps
A mixture of 2-bromobenzaldehyde (10.05 mmoles), 1-dodecyne (12.03 mmoles), cuprous iodide (0.11 mmoles) and bis(triphenylphosphine) palladium chloride (0.20 mmoles) in freshly distilled triethylamine (30 ml.) was heated for one hour at reflux producing a white precipitate. The reaction mixture was cooled and filtered. The filtrate was evaporated to dryness at reduced pressure and then dissolved in diethyl ether (50 ml) and washed with brine (50 ml). After treatment with anhydrous magnesium sulfate and charcoal, the solution was evaporated to afford a dark oil, which was purified by flash chromatography (2% Et2O/hexane) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04730005 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-5441687e730a4bf29b49401986ea30b6 |
| Source note | uspto-grants-1988_03 |