HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | 8-Methoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one | HCID 13520685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride | HCID 21242906 | — |
Reaction Steps
A suspension of 8-methoxy-2-oxo-2,3,4,5-tetrahydro-1H-3-benzazepine (20.4 g, 0.105 m) in tetrahydrofuran (500 ml) was added to 1 M borane in tetrahydrofuran (300 ml) stirred at 5°. The mixture was heated to reflux for 2 hours, cooled, treated with 3N hydrochloric acid (300 ml), concentrated in vacuo to remove tetrahydrofuran and heated to reflux for 1 hour. The mixture was concentrated in vacuo, filtered and the filter cake was dissolved in methanol, heated to reflux, dried with magnesium sulfate and concentrated in vacuo to afford 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride, m.p. 229°-231°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824839 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-c1675038d8f941d5ae3a67dbb80e24d3 |
| Source note | uspto-grants-1989_04 |