HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-Fluoro-4-trimethylsilylethynylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-Fluoro-4-trimethylsilylethynylbenzaldehyde | HCID 19990629 | — |
Reaction Steps
To a stirred solution of 4-bromo-3-fluorobenzaldehyde (6 g) in triethylamine (60 ml) was added trimethylsilylacetylene (4.6 ml), bis-triphenylphosphinepalladium dichloride (331 mg) and cuprous iodide (130 mg). The resulting mixture was allowed to stir overnight at room temperature under a nitrogen atmosphere. After this time, diethyl ether was added and the mixture was filtered. The filtrate was washed with water and brine before drying over anhydrous magnesium sulphate and evaporation in vacuo. The resulting oil was crystallised from cold hexane to give 3-fluoro-4-trimethylsilylethynylbenzaldehyde as a light brown solid (4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05061726 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-c5c33a142b1a4df7a961427205d29c26 |
| Source note | uspto-grants-1991_10 |