HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334528Generated: October 26, 2026
Phthalimide → 2-(4-(Pyridin-2-yl)but-3-ynyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/334528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl diazene-1,2-dicarboxylate | HCID 6034084 | — |
| Reactant | 4-(Pyridin-2-yl)but-3-yn-1-ol | HCID 11008063 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-(Pyridin-2-yl)but-3-ynyl)isoindoline-1,3-dione | HCID 11644791 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883826B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f0146874d1eb4dcaa09b9b791a2f3dd0 |
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| Source note | uspto-grants-2014_11 |
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