HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 10445614, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 5-Acetyl-2-hydroxy-6-methylnicotinonitrile | HCID 2765476 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 10445614 | HCID 10445614 | — |
Reaction Steps
A mixture of 3-cyano-5-acetyl-6-methyl-2(1H)-pyridinone (1.76 g, 0.01 mol) (L. Mosti et al, J. Het. Chem. 22, 1503 (1985)), benzyl bromide (2.12 g, 0.012 mol), silver carbonate (3.06 g, 0.011 mol) in benzene was stirred at room temperature under a nitrogen atmosphere overnight, while protected from light. The following day the mixture was filtered, and the solids washed well with benzene. Evaporation of the filtrate gave the desired intermediate, mp 94°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185251 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-991ed8f284b14acfa0eff7d6af92beff |
| Source note | uspto-grants-1993_02 |