HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic anhydride, 3-acetoxy- → 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic anhydride, 3-acetoxy- | HCID 294175 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Trifluoroacetic acid--3-aminopiperidine-2,6-dione (1/1) | HCID 53447112 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-acetoxyisoindoline | HCID 25015219 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853253B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-dc2da9662d7d4c2984161ee8c08bd700 |
| Source note | uspto-grants-2014_10 |