HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473518Generated: October 30, 2026
Phenylboronic Acid → 2-(5-(Biphenyl-3-yl)pent-4-ynyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/473518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-(5-(3-Bromophenyl)pent-4-ynyl)isoindoline-1,3-dione | HCID 67203127 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(5-(Biphenyl-3-yl)pent-4-ynyl)isoindoline-1,3-dione | HCID 67202488 | — |
Reaction Steps
2-(5-(3-Bromophenyl)pent-4-ynyl)isoindoline-1,3-dione (0.31 g, 0.84 mmol), phenyl boronic acid (206 mg, 1.68 mmol), and Pd (PPh3)4 (0.23, 0.2 mmol) were taken into DME (5 mL) and stirred at 80° C. for two hours. The reaction was then quenched with saturated NaHCO3 and the resulting mixture extracted with EtOAc, washed with brine, then dried over sodium sulfate and the solvent removed in vacuo. The resulting residue was purified on normal phase chromatography (Heptane/EtOAc) to yield 2-(5-(biphenyl-3-yl)pent-4-ynyl)isoindoline-1,3-dione. MH+ 366.3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633322B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-31c8c68df63946318ed47b271f9e3d1e |
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| Source note | uspto-grants-2014_01 |
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