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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367131Generated: November 1, 2026

3-Bromoaniline → HCID 86083506, compound

https://huagongshe.com/reaction/2367131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
ReactantDimethylacetamideHCID 31374—
ReactantHCID 86617517HCID 86617517—
ProductHCID 86083506HCID 8608350628%

Reaction Conditions

Temperature120 °C

Reaction Steps

Ethyl 4-chloro-4-(3,4-dinitrophenyl)butanone (366.3 mg, 1.2 mmol.), 3-bromoaniline (220 mg, 1.3 mmol.) and N,N-dimethylacetamide (0.3 mL) were combined and heated to 120° C. over 17 hours under a nitrogen atmosphere. The mixture was then cooled to room temperature and partitioned with ethyl acetate and water. The organic layer was washed twice with additional water, then brine and dried over anhydrous sodium sulfate. Filtration and concentration followed by purification of the residue by silica gel flash chromatography (100% ethyl acetate eluent) gave 1-(3-bromophenyl)-5-(3,4-dinitrophenyl)pyrrolidin-2-one (132 mg, 28% yield) as an amorphous residue. The material thus obtained is contaminated by variable amounts of 5-(3,4-dinitrophenyl)dihydrofuran-2(3H)-one as a side product and is carried forward without further purification. MS (EI) for C16H12N3O5Br: 407 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697737B2
Source datasetuspto-grants-2014_04
ORD IDord-c8effdf162fa4e4bb40ac58388eb5e81
Source noteuspto-grants-2014_04