Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533360Generated: October 26, 2026

Phthalic anhydride, 3-acetoxy- → 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindoline

https://huagongshe.com/reaction/533360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic anhydride, 3-acetoxy-HCID 294175—
ReactantSodium AcetateHCID 517045—
ReactantTrifluoroacetic acid--3-aminopiperidine-2,6-dione (1/1)HCID 53447112—
SolventAcetic AcidHCID 176—
Product1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindolineHCID 2501521966%

Reaction Steps

1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindoline was prepared and isolated as follows. A mixture of 3-acetoxyphthalic anhydride (40 mg), aminoglutarimide trifluoroacetate (47 mg), and NaOAc (32 mg) in acetic acid (2 mL) was refluxed for 5 h. The solvent was evaporated, water (10 mL) was added, and the resulting solution was stirred for several minutes. The solid was filtered out and recrystallized from ethyl acetate to give 1,3-dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindoline as pale yellow crystals (35 mg, 66%): 1H NMR (DMSO) δ 11.16 (s, 1H), 11.07 (s, 1H), 7.64 (t, J=7.2 Hz, 1H), 7.22-7.31 (m, 2H), 5.05 (dd, J=5.4 Hz, J=12.5 Hz, 1H), 2.87-2.92 (m, 2H), 2.48 (s, 3H), 2.08-2.00 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853253B2
Source datasetuspto-grants-2014_10
ORD IDord-dc2da9662d7d4c2984161ee8c08bd700
Source noteuspto-grants-2014_10