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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783682Generated: October 30, 2026

Phenylboronic Acid → HCID 178515029, compound

https://huagongshe.com/reaction/1783682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178515031HCID 178515031—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178515029HCID 17851502978%

Reaction Steps

4-Hydroxy-2-(4-iodophenyl)-2H-phthalazin-1-one (0.1 g, 0.3 mmol), phenyl boronic acid (0.04 g, 3 mmol), palladium black (0.02 g, 0.2 mmol) and KF (0.1 g, 18 mmol) were dissolved in MeOH (2 ml) and heated at reflux for 7 h. Removal of supernatant palladium by filtration, extraction with H2O and subsequent filtration of the precipitated solid yielded the desired title compound (0.07 g, 78% yield) as a white solid. 1H-NMR: (400 MHz, D6-DMSO) 11.88 (1H, s), 8.33 (1H, d), 7.89-8.03 (3H, m), 7.78-7.86 (6H, m), 7.50 (2H, t), 7.39 (1H, t),; MS (ESI+)=315.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501410B2
Source datasetuspto-grants-2009_03
ORD IDord-8bfa275789854f889496a16312b8b1e6
Source noteuspto-grants-2009_03