HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003697Generated: October 30, 2026
N-Carbethoxyphthalimide → 2-(4,4-Diethoxybutyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1003697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4,4-Diethoxybutyl)isoindoline-1,3-dione | HCID 12805186 | 104.1% |
Reaction Steps
A solution of 4-aminobutyraldehyde diethyl acetal (48.5 g, 0.3 mol) in tetrahydrofuran (60 ml) was added dropwise to a stirred slurry of N-(ethoxycarbonyl) phthalimide (65.93 g, 0.3 mol) in tetrahydrofuran (250 ml) at 0° C. After stirring at 0° C. for 0.16 h and at room temperature for 18 h the solvent was removed in vacuo and the residue distilled at 1 mmHg to remove the ethyl carbamate by-product. The residual brown oil was allowed to cool to afford the title compound (91 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046210 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-b7ebee8c1b7d419182063dd24fd4fa1d |
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| Source note | uspto-grants-2000_04 |
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