HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 18972163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18972171 | HCID 18972171 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18972163 | HCID 18972163 | — |
Reaction Steps
Ethyl 1,3,4,5-tetrahydro-benz[cd]indole-2-carboxylate (0.40 g, 1.74 mmol) was added to a suspension of 60% sodium hydride (0.077 g, 1.92 mmol) in N,N-dimethylformamide (5 ml), followed by stirring at room temperature for 30 minutes. Then, benzyl bromide (0.36 g, 2.09 mmol) was added and the resulting mixture was stirred for 1.5 hours. Thereafter, the same after-treatment as in Reference Example 1 was carried out to obtain an oil of ethyl 1,3,4,5-tetrahydro -1benzyl-benz[cd]indole-2-carboxylate. 1 Hnmr (CDC13) δ:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05814654 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-83832b6cfb4c48f1a6757c1dd0ae9712 |
| Source note | uspto-grants-1998_09 |