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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056629Generated: October 27, 2026

3a,4,5,7a-Tetrahydro-1H-isoindole-1,3(2H)-dione → Isoindole

https://huagongshe.com/reaction/1056629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3a,4,5,7a-Tetrahydro-1H-isoindole-1,3(2H)-dioneHCID 15277982—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductIsoindoleHCID 3013853—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of LAH (22.80 g, 600 mmol) in THF (600 mL) at 0° C. was added tetrahydrophthalimide (39.45 g, 260.9 mmol) portionwise. After addition, the reaction mixture was stirred at 60° C. for 18 h, then cooled down to 0° C. and quenched carefully with water (25 mL), followed by 15% KOH aqueous solution (25 mL) and another 75 mL of water. The resulting mixture was stirred at rt for 1 h and filtered through a pad of Celite, then washed with DCM (500 mL). The filtrate was concentrated in vacuo to give isoindole as yellow oil, which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399637B2
Source datasetuspto-grants-2016_07
ORD IDord-3b00c10b74d0495f8bef468d0c98ef0d
Source noteuspto-grants-2016_07