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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185951Generated: November 1, 2026

3,6-Dimethylphthalic anhydride → 2-(2,6-Dioxopiperid-3-yl)-4,7-dimethylisoindoline-1,3-dione

https://huagongshe.com/reaction/2185951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-Dimethylphthalic anhydrideHCID 21616—
Reactant3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product2-(2,6-Dioxopiperid-3-yl)-4,7-dimethylisoindoline-1,3-dioneHCID 9903976—

Reaction Steps

2-(2,6-Dioxopiperid-3-yl)-4,7-dimethylisoindoline-1,3-dione was prepared by the procedure of Example 1 from 3,6-dimethylphthalic anhydride (220 mg, 1.25 mmol), 3-aminopiperidine-2,6-dione hydrogen chloride (204 mg, 1.24 mmol) and sodium acetate (110 mg, 1.34 mmol) in acetic acid (10 mL). The product is a white solid (200 mg, 56% yield): mp 263.0-265.0° C.; 1H NMR (DMSO-d6) δ2.01-2.07 (m, 1H, CHH), 2.50-2.89 (m, 9H, CH3, CHH, CH2), 5.10 (dd, J=5.1, 12.4 Hz, 1H, NCH), 7.52 (s, 2H, Ar), 11.12 (br s, 1H, NH); 13C NMR (DMSO-d6) δ16.82, 22.02, 30.97, 48.59, 128.01, 135.04, 136.58, 167.68, 169.98, 172.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403613B1
Source datasetuspto-grants-2002_06
ORD IDord-1eaf15b25b704b05a552b8fc2e4b7a8e
Source noteuspto-grants-2002_06