HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → HCID 19347933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Phenyl-1,4-diazepan-5-one | HCID 13048235 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19347933 | HCID 19347933 | 83.9% |
Reaction Steps
1.9 g hexahydro-7-phenyl-1,4-diazepin-5-one (for preparation see Example 1C) in 30 ml acetonitrile were heated to boiling with 2.0 g potassium carbonate and 1.2 g benzyl chloride with reflux cooling for 36 hours. Then filtration was carried out and the filtrate reduced in volume. The remaining residue was shaken with 10% aqueous citric acid solution, the organic phase was separated, dried over magnesium sulfate and reduced in volume under a vacuum. 2.23 g crude 1-benzyl-hexahydro-7-phenyl-1,4-diazepin-5-one were obtained as an oil, which was used for the next synthesis stage without further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06040303 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-6d0163b8cb4649f29ae48e11f811ce12 |
| Source note | uspto-grants-2000_03 |