HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 4-[(5-Nitro-thien-2-yl)ethynyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-5-nitrothiophene | HCID 83222 | — |
| Reactant | 4-Ethynylbenzonitrile | HCID 4547245 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[(5-Nitro-thien-2-yl)ethynyl]benzonitrile | HCID 19691953 | — |
Reaction Steps
To a solution of 4-ethynylbenzonitrile (0.5 g), 2-bromo-5-nitrothiophene (0.9 g) and bis(triphenylphosphine)palladium dichloride (83 mg) in anhydrous dimethylformamide (4 ml) was added triethylamine (2.2 ml). The reaction mixture was stirred at room temperature for 3 days then ethyl acetate (200 ml) and saturated sodium chloride (200 ml) were added. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The crude solid was triturated with 1:1 dichloromethane/hexane followed by diethyl ether to give 4-[(5-nitro-2-thienyl)ethynyl]benzonitrile as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726195 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-f537d62089cd4cba9bc833054c2f705b |
| Source note | uspto-grants-1998_03 |