HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647889Generated: October 29, 2026
Iodine → 3-Bromo-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one
https://huagongshe.com/reaction/647889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one | HCID 248580 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Bromo-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one | HCID 2757184 | — |
Reaction Steps
To a solution of 2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one (2.5 g) in chloroform (30 ml), phosphorus pentachloride (3.2 g) was added in portions, while maintaining the temperature at 0°-5°. When the addition was complete, iodine (30 mg) was added followed by bromine (2.5 g), which was added dropwise over 5 minutes. The mixture was then refluxed for 4 hours. The chloroform solution was evaporated and the residue was partitioned between ice-water (30 ml) and dichloromethane (75 ml). The organic phase was dried over magnesium sulfate and evaporated under reduced pressure. The crude residue was purified by chromatography over silica gel, eluting with ether and hexane (7:3). Concentration of the appropriate fractions yielded 3-bromo-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one, m.p. 146°-148°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04410520 |
|---|
| Source dataset | uspto-grants-1983_10 |
|---|
| ORD ID | ord-760be246e2384bef82f54e089596e8f4 |
|---|
| Source note | uspto-grants-1983_10 |
|---|