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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898872Generated: October 30, 2026

Phthalic Anhydride → HCID 68860699, compound

https://huagongshe.com/reaction/898872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantSodium hydrideHCID 24758—
Reactant5-Methoxy-2,3-dihydro-1H-inden-2-aMine hydrochlorideHCID 67160966—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68860699HCID 6886069943%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351857B2
Source datasetuspto-grants-2008_04
ORD IDord-d184820f5f8540f3a30a6ceeab573a51
Source noteuspto-grants-2008_04