HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1H-1-Benzazepine, 2,3,4,5-tetrahydro-1-(4-nitrobenzoyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 2,3,4,5-tetrahydro-1H-1-benzazepine | HCID 576503 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1H-1-Benzazepine, 2,3,4,5-tetrahydro-1-(4-nitrobenzoyl)- | HCID 10637676 | 77% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 5.0 g of 1,2,3,4-tetrahydro-5H-1-benzazepine and 5.91 ml of triethylamine in 50 ml of dichloromethane, chilled in an ice bath, is added, dropwise, 6.32 g of 4-nitrobenzoyl chloride in 75 ml of dichloromethane. The mixture is stirred at 0° C. for 1.5 hr and then at room temperature for 18 hours. The mixture is washed with H2 O, 2M HCl, 1M NaOH and dried (Na2SO4). The solvent is removed and the residue recrystallized from ethanol with the aid of activated carbon to give 7.75 g of light yellow crystals, m.p. 148.5°-150.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760031 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-077c6cf8979f41608d8dff5974954931 |
| Source note | uspto-grants-1998_06 |