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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75374Generated: October 29, 2026

Water → 2-(1-(3,5-Dichloroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/75374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPhthalimide potassium saltHCID 24194345—
Reactant2-(1-Bromoethyl)-3,5-dichloroquinoxalineHCID 86698511—
SolventDimethylformamideHCID 6228—
Product2-(1-(3,5-Dichloroquinoxalin-2-yl)ethyl)isoindoline-1,3-dioneHCID 86698512101.9%

Reaction Steps

To a solution of 2-(1-bromoethyl)-3,5-dichloroquinoxaline (1.00 Kg, 3.27 mol) in DMF (8.2 L) was added potassium phthalimide (1.21 Kg, 6.54 mol). The reaction mixture was stirred for 3 h. At this time LC-MS analysis showed that the reaction was complete. The mixture was transferred to a 50 L separatory funnel and water (12 L) and EtOAc (6 L) were added to it with stirring. A large amount of white solid crashed out and was collected by filtration. The aqueous. phase was separated and extracted again with EtOAc (2×4 L). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, and the volume was reduced to 5 L under reduced pressure. After cooling to rt, the product was obtained as a white solid. The white solid was filtered, triturated with hexane and dried under vacuum to give 2-(1-(3,5-dichloroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione (1.24 Kg). 1H NMR (DMSO-d6) δ ppm 8.02-8.21 (2H, m), 7.83-8.02 (m, 5H), 5.89 (q, J=6.8 Hz, 1H), 1.87 (d, J=6.8 Hz, 3H). Mass Spectrum (ESI) m/z=372.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835432B2
Source datasetuspto-grants-2014_09
ORD IDord-ebc37859c39c4cfb984781b31f2aef87
Source noteuspto-grants-2014_09