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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891983Generated: October 29, 2026

4-Methyl-1,3-isobenzofurandione → 3-(4-Methyl-1,3-dioxoisoindolin-2-yl)-2,6-dioxo-5-acetoxypiperidine

https://huagongshe.com/reaction/891983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-1,3-isobenzofurandioneHCID 98500—
ReactantHCID 12047333HCID 12047333—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product3-(4-Methyl-1,3-dioxoisoindolin-2-yl)-2,6-dioxo-5-acetoxypiperidineHCID 12047334—

Reaction Steps

A mixture of 2,6-dioxo-3-benzyloxycarbonylamino-5-acetoxypiperidine (9 g, 28.2 mmol) (U. Teubert et al, Arch. Pharm. Pharm. Med. Chem. (1998) 7–12) and Pd/C (10%, 0.9 g) in acetic acid (90 mL) is shaken under hydrogen (50–60 psi) for 3 hours. The suspension is filtered through a pad of Celite and washed with acetic acid. To the filtrate is added 3-methylphthalic anhydride (4.56 g, 28.2 mmol) and this mixture is heated at reflux for 18 hours. The solvent is removed in vacuo to give 3-(4-methyl-1,3-dioxoisoindolin-2-yl)-2,6-dioxo-5-acetoxypiperidine which can be further purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005438B2
Source datasetuspto-grants-2006_02
ORD IDord-794f7db6c22b4df3adef3dbfcfb6b9be
Source noteuspto-grants-2006_02