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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901278Generated: October 25, 2026

Methane → 2-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1901278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,5-HexanedioneHCID 8035—
ReactantN-AminophthalimideHCID 74645—
SolventTolueneHCID 1140—
Product2-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 2817169—

Reaction Steps

A stirred suspension of N-aminophthalimide (19.75 g), acetonylacetone (14.3 ml), p-toluenesulfonic acid (5 mg), and toluene (406 ml) was heated at reflux for 1 hour and cooled to room temperature. The reaction mixture was combined with another reaction mixture and the entire mixture decolorized with activated charcoal. Filtration through a bed of celite gave a solution which upon partial concentration resulted in crystallization of the desired product as a solid (11.0 g), m.p. 182.5°-183.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576446
Source datasetuspto-grants-1996_11
ORD IDord-cab0f115ffce47b6808536d1da0e37a5
Source noteuspto-grants-1996_11