Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189055Generated: October 31, 2026

Phthalimide → 2-(4-(Pyridin-2-yl)but-3-ynyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1189055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
Reactant4-(Pyridin-2-yl)but-3-yn-1-olHCID 11008063—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(4-(Pyridin-2-yl)but-3-ynyl)isoindoline-1,3-dioneHCID 1164479173%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(Pyridin-2-yl)but-3-yn-1-ol (96 mg, 0.65 mmol), isoindoline-1,3-dione (140 mg, 0.97 mmol) and triphenylphosphine polymer bound 3 mmol/g (340 mg, 1.02 mmol) were dissolved in DCM (2 mL) and cooled to 0° C. Di-tert-butylazodicarboxylate (226 mg, 0.96 mmol) dissolved in DCM (0.5 mL) was added dropwise over 30 min. to the reaction mixture followed by THF (0.5 mL) and the reaction mixture was stirred for 16 h at room temperature. After filtration through celite, the organic phase was washed with a solution of NH4OH, brine, dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 3:7) to yield 130 mg (0.47 mmol, 73%) of 2-(4-(pyridin-2-yl)but-3-ynyl)isoindoline-1,3-dione as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-9e1373852e234fc7b16cec6fce755f4c
Source noteuspto-grants-2014_03