HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477981Generated: October 27, 2026
3a,4,5,7a-Tetrahydro-1H-isoindole-1,3(2H)-dione → Isoindole
https://huagongshe.com/reaction/1477981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3a,4,5,7a-Tetrahydro-1H-isoindole-1,3(2H)-dione | HCID 15277982 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Isoindole | HCID 3013853 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403801B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-bfd6e51c7166434185ceb110919f7c44 |
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| Source note | uspto-grants-2016_08 |
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