HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898872Generated: October 30, 2026
Phthalic Anhydride → HCID 68860699, compound
https://huagongshe.com/reaction/898872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methoxy-2,3-dihydro-1H-inden-2-aMine hydrochloride | HCID 67160966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68860699 | HCID 68860699 | 43% |
Reaction Steps
To a suspension of 60% NaH (8 g; 0.240 mol) in DMF (250 mL), cooled to 0° C., is added 5-methoxyindan-2-ylamine hydrochloride (40.0 g; 0.2 mol) and the suspension stirred for 1 h at RT. Phthalic anhydride (30 g; 0.2 mol) is added in 1-portion and the suspension stirred for an additional 1-1.5 h at RT followed by stirring at 120° C. for 96 h. The reaction is cooled and diluted with EtOAc. The organic phase is washed with H2O, the resultant precipitate filtered, washed with EtOAc, MeOH and dried under vacuo to afford 25.2 g (43%) of 2-(5-methoxyindan-2-yl)isoindole-1,3-dione as a white solid. The organic phase is washed with H2O, evaporated under reduced pressure and the solid is triturated with MeOH, filtered, and dried to afford an additional 19.7 (33%) g of 2-(5-methoxyindan-2-yl)isoindole-1,3-dione as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351857B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-d184820f5f8540f3a30a6ceeab573a51 |
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| Source note | uspto-grants-2008_04 |
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