Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant2-(5-(3-Bromophenyl)pent-4-ynyl)isoindoline-1,3-dioneHCID 67203127—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(5-(Biphenyl-3-yl)pent-4-ynyl)isoindoline-1,3-dioneHCID 67202488—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633322B2
Source datasetuspto-grants-2014_01
ORD IDord-31c8c68df63946318ed47b271f9e3d1e
Source noteuspto-grants-2014_01