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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalimideHCID 6809—
Edukt10-Undecen-1-olHCID 8185—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699467B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-6138fbfac24d447199213a4fb085e741
Quellennotizuspto-grants-2004_03