HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717346Generated: October 30, 2026
Beta-Alanine → 3-Phthalimidopropionic acid
https://huagongshe.com/reaction/717346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Beta-Alanine | HCID 239 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Phthalimidopropionic acid | HCID 76859 | — |
Reaction Steps
Into a 3-L 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-aminopropanoic acid (20 g, 224.48 mmol, 1.00 equiv) and 1,3-dihydro-2-benzofuran-1,3-dione (33.28 g, 224.69 mmol, 1.00 equiv) in acetic acid (1,200 mL). This was followed by the addition of potassium acetate (66.0 g, 672.49 mmol, 3.00 equiv) in several batches at 0° C. The resulting solution was stirred for 3 h at 80° C. in an oil bath. The resulting mixture was concentrated under vacuum. The reaction was then quenched by the addition of 150 mL of water. The solids were collected by filtration. This resulted in 40 g (81%) of 3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid as a white solid. Rf: 0.15 (in ethyl acetate:petroleum ether=1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193707B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-27ecbc891b4e4747bef677d8508bff9d |
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| Source note | uspto-grants-2015_11 |
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