HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284358Generated: October 30, 2026
Hydrochloric Acid → 11-Chloro-2-methyl-2,3-dihydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrol-1-one
https://huagongshe.com/reaction/2284358
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Bromhydrol | HCID 166749 | — |
| Reactant | 3-(5-Chloro-2-phenoxyphenyl)-1-methylpyrrolidine-2,4-dione | HCID 57826927 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 11-Chloro-2-methyl-2,3-dihydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrol-1-one | HCID 10357298 | — |
Reaction Steps
Anhydrous aluminium bromide (2.5 g) was added to a reaction mixture containing 3-(5-chloro-2-phenoxyphenyl)-1-methylpyrrolidine-2,4-dione (1 g) in 1,2-dichlorobenzene (4 mL) at ambient temperature. The reaction mixture was stirred at about 85° C. for about 9 hours, then cooled to ambient temperature. A mixture of water and concentrated hydrochloric acid (50 mL:5 mL) was added slowly. The contents were stirred for about 30 minutes. Hexane (10 mL) was added. The contents were stirred for about 1 hour, filtered, washed with hexane (10 mL) and dried in air at about 30° C. for about 15 hours to obtain 11-chloro-2-methyl-2,3-dihydro-1H-dibenzo [2,3:6,7]oxepino[4,5-c]pyrrol-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145421B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-67eb6d69493a4e2d895a6d6260032cc9 |
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| Source note | uspto-grants-2015_09 |
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