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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037193Generated: November 2, 2026

Acetic Acid → 4-(i-Propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-one

https://huagongshe.com/reaction/2037193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethoxybenzaldehydeHCID 8658—
Reactant4-(Thiophen-3-yl)anilineHCID 4130336—
ReactantMethyl 3-(i-propylsulfonyl)-2-oxopropanoateHCID 58365407—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-(i-Propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-oneHCID 5836531679%

Reaction Steps

A mixture of methyl 3-(i-propylsulfonyl)-2-oxopropanoate (0.23 g, 1 mmol), 4-thiophene-3-ylaniline (0.18 g, 1 mmol), 2-methoxybenzaldehyde (0.14, 1 mmol), acetic acid (0.023 mL, 0.4 mmol) and toluene (3 mL) was heated at reflux overnight. After the reaction was completed, the reaction mixture was allowed to cool to room temperature. To the mixture was added ether and precipitated compound was collected by filtration. The resulting aimed compound was washed with ether/n-hexane solution to give 4-(i-propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-one (0.37 g, yield: 79%) as pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575197B2
Source datasetuspto-grants-2013_11
ORD IDord-b602de288ce0466ebacf50b38907cb85
Source noteuspto-grants-2013_11