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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47155Generated: October 26, 2026

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

https://huagongshe.com/reaction/47155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
Reactant10-Undecen-1-olHCID 8185—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
Product2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 22044522—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699467B2
Source datasetuspto-grants-2004_03
ORD IDord-6138fbfac24d447199213a4fb085e741
Source noteuspto-grants-2004_03