HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226840Generated: November 2, 2026
2-Bromobenzonitrile → HCID 18963827, compound
https://huagongshe.com/reaction/2226840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromobenzonitrile | HCID 16272 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18963827 | HCID 18963827 | 114% |
Reaction Steps
The title D compound (1.99 g, 9.00 mmol) was dissolved in 10 mL of freshly distilled tetrahydrofuran, cooled to -78° C. and n-butyllithium (2.23M in hexane, 4.24 mL, 9.45 mmol) was added dropwise over 10 minutes. Upon complete addition the reaction was cloudy, bright yellow. After stirring 40 minutes, zinc chloride (1.0M in ether, 9.45 mL, 9.45 mmol) was added and the reaction mixture turned to clear pale yellow. The reaction was stirred 30 minutes, then the cold bath was removed and the reaction stirred an additional 30 minutes before 2-bromobenzonitrile (1.64 g, 9.45 mmol) and tetrakis(triphenylphosphine)palladium(O) (520 mg, 0.45 mmol) were added. After stirring 22 hours at 55° C., the reaction mixture was adsorbed on 10 g of silica gel and purified by flash chromatography (170 g silica gel; 30% toluene, hexane) to yield 1.31 g (60%) of the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05350752 |
|---|
| Source dataset | uspto-grants-1994_09 |
|---|
| ORD ID | ord-700b42dd6ae54680b2dccba366454f52 |
|---|
| Source note | uspto-grants-1994_09 |
|---|