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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48224Generated: October 30, 2026

4-amino-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione → HCID 21138365, compound

https://huagongshe.com/reaction/48224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-amino-2-methyl-2,3-dihydro-1H-isoindole-1,3-dioneHCID 600596—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21138365HCID 2113836585.5%

Reaction Steps

A 5-L flask was set up with an overhead stirrer, temperature probe, and 500-mL addition funnel. The flask was charged with lithium aluminum hydride (100 g) and anhydrous tetrahydrofuran (1.5 L). The resulting suspension was treated with 4-amino-2-methyl-1H-isoindole-1,3(2H)-dione (100 g, 0.56 mol) at a rate such that the reaction did not become too vigorous. The resulting suspension was heated at reflux for 18 hours. The reaction vessel was cooled, placed in an ice bath, and cautiously quenched with 100 mL water, 100 mL 1N NaOH, and 300 mL water. The resulting suspension was treated with chloroform (1.5 L) and the pH of the suspension adjusted to 12 with 50% aqueous sodium hydroxide solution. The resulting suspension was treated with acetic anhydride (300 mL) while maintaining the pH at approximately 12. The reaction mixture was treated with sodium sulfate (800 g) and potassium carbonate (200 g), and the reaction mixture was filtered. The filter cake was washed with additional chloroform, and the combined filtrates were concentrated. The residue was crystallized from ethyl acetate to give 71 g (66%) of the desired product, mp 157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703391B2
Source datasetuspto-grants-2004_03
ORD IDord-5c2303aceddb4f00b6cef28bc26677e1
Source noteuspto-grants-2004_03