HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464931Generated: October 30, 2026
HCID 13556875, compound → 8-Chloro-4,5-dihydro-1-phenyl-3H-2-benzazepine hydrochloride
https://huagongshe.com/reaction/464931
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13556875 | HCID 13556875 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 8-Chloro-4,5-dihydro-1-phenyl-3H-2-benzazepine hydrochloride | HCID 13556878 | — |
Reaction Steps
A solution of 5.1 g (12.6 mmole) of 1-[4-chloro-2-benzoylphenyl]-3-phthalimidopropane in 100 ml of ethanol and 20 ml of 3N sodium hydroxide was refluxed for 2 hr. The solution was diluted with 60 ml of 3N hydrochloric acid and refluxed for 12 hr. The mixture was diluted with water and extracted with ether. The aqueous layer was separated, made alkaline with dilute sodium hydroxide, and extracted with methylene chloride. The methylene chloride extract was dried over anhydrous sodium sulfate and concentrated at reduced pressure to dryness. The residue was purified by plug filtration (silica gel, 10 g; eluent, methylene chloride) and the eluent was acidified with methanolic hydrogen chloride. The solution was concentrated at reduced pressure to dryness and the residue was crystallized from a mixture of isopropanol and ether to give a colorless solid, mp 234°-235° C. Recrystallization from a mixture of methylene chloride and ether gave colorless needles, mp 234°-235° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04549988 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-fa7777c9d5a244d3933badd18e903767 |
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| Source note | uspto-grants-1985_10 |
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