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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749527Generated: November 2, 2026

Phthalic Anhydride → 2-(2-(2-Oxoindolin-3-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1749527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
Reactant3-(2-aminoethyl)-2,3-dihydro-1H-indol-2-one hydrochlorideHCID 11701292—
Solventtoluene N-methylpyrrolidoneHCID 21877177—
Product2-(2-(2-Oxoindolin-3-yl)ethyl)isoindoline-1,3-dioneHCID 11816210856.4%

Reaction Steps

A mixture of 3-(2-aminoethyl)indolin-2-one hydrochloride (3.20 g, 15.06 mmol), phthalic anhydride (3.34 g, 22.59 mmol) and TEA (4.56 g, 45.18 mmol) in toluene/NMP (20 mL/10 mL). The mixture was heated under reflux for 3 h. The reaction mixture was concentrated and the resulting mixture was washed with saturated aqueous ammonium chloride and brine. The separated organic layer was dried over anhydrous sodium sulfate and filtered. Concentration under vacuum gave the crude product, which was purified by silica gel column chromatography (30% ethyl acetate in petroleum ether) to afford the title compound (2.60 g, 8.50 mmol, 56% yield) as a brown solid. MS (ESI) m/z 307.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156798B2
Source datasetuspto-grants-2015_10
ORD IDord-461153b79e1e45dba12ce8d99d44aadf
Source noteuspto-grants-2015_10