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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantBromhydrolHCID 166749—
Reactant3-(5-Chloro-2-phenoxyphenyl)-1-methylpyrrolidine-2,4-dioneHCID 57826927—
Solvent1,2-DichlorobenzeneHCID 7239—
SolventHexaneHCID 8058—
Product11-Chloro-2-methyl-2,3-dihydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrol-1-oneHCID 10357298—

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145421B2
Source datasetuspto-grants-2015_09
ORD IDord-67eb6d69493a4e2d895a6d6260032cc9
Source noteuspto-grants-2015_09