HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 19769112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 19769113 | HCID 19769113 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19769112 | HCID 19769112 | — |
Reaction Steps
To a partial suspension of 3-cyano-5-ethyl-6-benzyloxymethyl-2(1H)-pyridinone (1.36 g, 5.08 mmol) in dry benzene (20 mL) was added benzyl bromide (0.80 mL, 6.7 mmol) and then silver carbonate (1.43 g, 5.2 mmol). This mixture was covered with aluminum foil and allowed to stir at room temperature. After 24 hours, the reaction was estimated to be ~80% complete. Additional silver carbonate (0.40 g, 1.45 mmol) was added and the mixture was stirred for another 24 hours until complete. The silver salts were removed by filtration, rinsed with benzene and the combined benzene washings were evaporated to give the pure product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185251 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-3fea9745d05d4acb9bd5e99286fb2f27 |
| Source note | uspto-grants-1993_02 |