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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611450Generated: November 1, 2026

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

https://huagongshe.com/reaction/611450

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 numberUS06001347
Source datasetuspto-grants-1999_12
ORD IDord-5c33937d4f2c44399de887c7314c4cb1
Source noteuspto-grants-1999_12