HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-chloro-1-(9H-tribenz[b,d,f]azepine-9-yl)propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 9H-Tribenzo[b,d,f]azepine | HCID 11299519 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-chloro-1-(9H-tribenz[b,d,f]azepine-9-yl)propan-1-one | HCID 18917169 | 94% |
Reaction Steps
9H-Tribenz[b,d,f]azepine (0.17 g, 0.70 mmol, prepared similarly as described by H. C. Axtell et al., J. Org. Chem. 56, 3906 (1991)) was suspended in dry toluene (5 ml). 3-Chloropropionyl chloride (0.13 g, 1.0 mmol) and triethylamine (0.1 ml) were added and the mixture was heated at reflux temperature for 1.5 hour. Saturated aqueous sodium bicarbonate (10 ml) was added, and the phases were separated. The organic phase was washed with brine (10 ml), dried (MgSO4) and concentrated in vacuo, affording 220 mg, (94%) of crude 3-chloro-1-(9H-tribenz[b,d,f]azepine-9-yl)propan-1-one as a foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716949 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-389372046bb14407b7543b0b2c5210e3 |
| Source note | uspto-grants-1998_02 |