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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7336Generated: October 23, 2026

Potassium Carbonate → 1-Phenylisoquinoline

https://huagongshe.com/en/reaction/7336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-ChloroisoquinolineHCID 21989390—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-PhenylisoquinolineHCID 13788296.9%

Reaction Steps

2-Chloro-isoquinoline (28.8 g, 0.176 mol), phenylboronic acid (25.7 g 0.211 mol), triphenylphosphine (4.6 g 17.6 mmol), palladium acetate (0.99 g 4.4 mmol) and 2M solution of potassium carbonate (65.7 g 0.475 mol) were added to 270 ml of dimethoxyethane. This mixture was stirred at reflux for 17 hrs. The mixture was then cooled and the aqueous layer was separated from the organic layer. The aqueous extraction was then extracted with ethyl acetate. The combined organic extractions were then extracted with brine and dried over magnesium sulfate. The solvent was then evaporated to give a liquid which was then purified by Kugelhor distillation at 220° C. @1200 microns to yield 35 g (96.9%) of 1-phenylisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087321B2
Source datasetuspto-grants-2006_08
ORD IDord-d9f85d7ffa8444e78678cc9498e7bd8a
Source noteuspto-grants-2006_08