HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 13383905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl Beta-Carboline-3-Carboxylate | HCID 105078 | — |
| Reactant | HCID 11404295 | HCID 11404295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13383905 | HCID 13383905 | 70% |
Reaction Steps
Ethyl β-carboline-3-carboxylate 10 (4.8 g, 20 mmol), DMF (100 ml) and THF (100 ml) were respectively added in a 100 ml round-bottom flask, and were stirred at room temperature for 15 minutes, then 60% NaH (2.4 g, 60 mmol) was added and stirred until there were no bubbles formed. Benzyl bromide (15 ml) was added, and the mixture was refluxed for 12 h. Later the mixture was treated in a manner similar to that described for compound 29 to afford white crystals (4.6 g, 70%), mp 126-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772311B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-530e5aaac78a4cd8a12a7adae92b7627 |
| Source note | uspto-grants-2014_07 |