HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47155Erstellt: 23. Oktober 2026
Phthalimide → 2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/de/reaction/47155
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phthalimide | HCID 6809 | — |
| Edukt | 10-Undecen-1-ol | HCID 8185 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dione | HCID 22044522 | — |
Reaktionsschritte
A mixture of 10-undecene-1-ol (5.00 g, 29.36 mmol, 1 equiv), triphenylphosphine (7.70 g, 29.36 mmol, 1 equiv) and phthalimide (4.32 g, 29.36 mmol, 1 equiv) in dry tetrahydrofuran (THF, 30 mL) was stirred vigorously under argon. Diethyl azodicarboxylate (DEAD, 5.11 g, 29.36 mmol, 1 equiv) was diluted with THF (12 mL) and added dropwise by syringe. After the addition, the reaction was stirred at room temperature for 4 hours. The solvent was evaporated under vacuum and ether (30 mL) was added to precipitate the triphenylphosphine oxide and hydrazine dicarboxylate which were removed by filtration. The precipitate was rinsed with ether (2×30 mL) and the combined filtrates were evaporated to afford a yellow solid. The yellow solid was triturated with warm hexanes (3×50 mL) and filtered. The combined hexanes were evaporated to give 1-phthalimidylundec-10-ene as a yellow wax.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06699467B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-6138fbfac24d447199213a4fb085e741 |
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| Quellennotiz | uspto-grants-2004_03 |
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