HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647871Generated: October 30, 2026
Hydrochloric Acid → HCID 13243503, compound
https://huagongshe.com/reaction/647871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 8-methoxy-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one | HCID 676953 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 13243503 | HCID 13243503 | — |
Reaction Steps
A solution of 8-methoxy-2,3,4,5-tetrahydro-1H [1]benzazepin-2-one (7.0 g, described in Example 14) and phosphorous pentachloride (30.0 g) in xylene (200 ml) was heated with stirring under an atmosphere of nitrogen to 90° (oil bath temperature) during 30 minutes with pauses at 30° and at 50°. There was a copious evolution of hydrogen chloride gas. The temperature was maintained at 90° for 30 minutes. The reaction mixture was filtered while hot to remove a small amount of suspended solid, and the filtrate was evaporated under reduced pressure until all the solvent was removed. The residue was added with stirring to saturated aqueous sodium carbonate (20 ml). The product was filtered after the solidification process was complete, slurried in ethanol (30 ml), washed with ethanol (10 ml) and ether (10 ml) and dried to give 3,3-dichloro-8-methoxy-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 148°-150°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410520 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-69765b388aa94dbaa89f96350fa7a444 |
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| Source note | uspto-grants-1983_10 |
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