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HRID 488480Erstellt: 24. Oktober 2026

Phthalimide → 2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/de/reaction/488480

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
PatentnummerUS06972300B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-35529dfd240e4e52867eade359e02e4d
Quellennotizuspto-grants-2005_12