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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614696Generated: November 1, 2026

Oxalyl chloride → 4-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoyl chloride

https://huagongshe.com/reaction/1614696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)benzoic acidHCID 86925—
SolventBenzeneHCID 241—
Product4-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoyl chlorideHCID 13365404—

Reaction Steps

Para-maleimidobenzoyl chloride was prepared in accordance with the procedure described by Adams et al. in J. Am. Chem. Soc , 42, 599 (1920). The N-(para-carboxyphenyl) maleimide (15 g) was suspended in about 80 ml of benzene with stirring. To this mixture was added 15 ml (a 2.5:1 molar excess) of oxalyl chloride, whereupon some gas was evolved. The mixture was then heated slowly to reflux and maintained at reflux for two hours. Excess oxalyl chloride was removed by distillation. The reaction mixture was then cooled and the yellow product recovered by suction filtration. The resultant product was washed with hexane and dried under vacuum at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198551
Source datasetuspto-grants-1993_03
ORD IDord-18d86bbc782e4c05af8269f2446f5e8a
Source noteuspto-grants-1993_03