HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22563201, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22563201 | HCID 22563201 | 100% |
Reaction Steps
To a solution of 4-cyanophenacyl bromide (10) (5.02 g, 22.2 mmol) in anhydrous acetonitrile (300 mL) was added pyridine (3.6 mL, 45.3 mmol) at room temperature. The mixture was stirred for 30 minutes. The precipitate was filtrated, washed with acetonitrile (20 mL) and dried under vacuum to give 1-(2-(4-cyano-phenyl)-2-oxo-ethyl)-pyridinium bromide (11) as a white powder (100%). 1H NMR (DMSO-d6) δ 6.56 (s, 2H), 8.21 (m, 6H), 8.76 (t, J=7.8, 1H), 9.03 (d, J=6.6, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861436B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-64abd064b57b4fa28fc1d90b5510fb45 |
| Source note | uspto-grants-2005_03 |