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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556295Generated: October 26, 2026

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

https://huagongshe.com/reaction/556295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
Reactant10-Undecen-1-olHCID 8185—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
Product2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 2204452266%

Reaction Steps

To a mixture of 10-undecen-1-ol (4.23 g, 24.8 mmol), phthalimide (3.65 g, 24.8 mmol) and triphenylphosphine (6.51 g, 24.8 mmol) in anhydrous tetrahydrofuran (30 ml), a solution of DEAD (3.9 ml, 24.8 mmol) in anhydrous tetrahydrofuran (10 ml) was slowly added while keeping the temperature below 8-10° C. After 2 hours further DEAD (1.0 ml, 6.37 mmol) and triphenylphosphine (1.3 g, 4.96 mmol) were added and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated and the residue was triturated with diethyl ether (50 ml). The solid was removed by filtration and washed with diethyl ether (2×50 ml). The combined filtrates were concentrated and the residue was triturated with hexane (50 ml) at 40° C. The resulting solid was removed by filtration and washed with hexane (2×50 ml). The combined filtrates were concentrated and the residue was purified by column chromatography eluting with 10:2 hexane:ethyl acetate mixture. The product was obtained as a low-melting white solid (4.9 g, 66% yield). M.p. 25-30° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058262B2
Source datasetuspto-grants-2011_11
ORD IDord-dcaeb53e05d64582beed6da5aee9ebd8
Source noteuspto-grants-2011_11