HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 6-Bromonaphthalene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 6-Bromo-2-naphthamide | HCID 57428037 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Bromonaphthalene-2-carbonitrile | HCID 14662115 | 70.3% |
Reaction Steps
To 6-bromo-2-naphthamide (1 g, 4.00 mmol) in dioxane (8.00 ml) at 0° C. was added pyridine (0.647 ml, 8.00 mmol) and then TFAA (0.621 ml, 4.40 mmol) dropwise. The reaction was stirred at room temperature for 3 h. The mixture was quenched with H2O and extracted with EtOAc two times, dried over magnesium sulfate, filtered, concentrated. The title compound (653 mg, 70%) was isolated as a beige solid, and used as is for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383827B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-738b927a24984ec88ef771e83a58ff18 |
| Source note | uspto-grants-2013_02 |