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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084985Generated: October 26, 2026

3-Bromoaniline → 3-(3-Bromophenylamino)-4-(4-chlorophenyl)-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/2084985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
Reactant3-chloro-4-(4-chlorophenyl)-1H-pyrrole-2,5-dioneHCID 11287952—
SolventMethanolHCID 887—
Product3-(3-Bromophenylamino)-4-(4-chlorophenyl)-1H-pyrrole-2,5-dioneHCID 9951668—

Reaction Steps

A solution of 3-bromoaniline (227 mL, 0.020 mol) and 3-chloro-4-(4-chlorophenyl)-1H-pyrrole-2,5-dione (2.02 g, 0.0083 mol; prepared by analogy with the methods described in WO97/34890 and Wiley, R P H, and Slaymaker, S. C. J. Am. Chem. Soc (80) 1385 (1958)) in methanol (50 mL) was heated at reflux for 40 hours, cooled and concentrated. The residue was acidified with aqueous hydrochloric acid (1M, 200 mL) and extracted with ethyl acetate (3×200 mL). The combined organic solutions were washed with water and brine, dried with magnesium sulphate, evaporated and the residue chromatographed on silica gel using dichloromethane-diethyl ether (gradient from 100:0 to 95:5 v/v) as eluent to afford the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06719520B2
Source datasetuspto-grants-2004_04
ORD IDord-b98e98e237b141459aae2a73dbad1912
Source noteuspto-grants-2004_04