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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004297Generated: October 30, 2026

Potassium Carbonate → HCID 54255487, compound

https://huagongshe.com/reaction/1004297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 54554919HCID 54554919—
SolventTolueneHCID 1140—
ProductHCID 54255487HCID 54255487—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a stirred solution of 9-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)-3-(trifluoromethanesulfonyloxy)-non-2-enoic acid tert-butyl ester 29-6 (100 mg, 0.20 mmol) in toluene (2.5 mL) was added palladium(tetrakis)-triphenylphosphine (23 mg, 0.020 mmol), phenylboronic acid (50 mg, 0.41 mmol), and potassium carbonate (56 mg, 0.41 mmol). The resulting suspension was heated at 90-100° C. for 2 hours, and then was allowed to cool to ambient temperature. The reaction mixture was then poured into saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried with anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The resulting oil was purified by flash column chromatography over silica gel with 4:1 ethyl acetate/hexanes to give 29-7a as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048861
Source datasetuspto-grants-2000_04
ORD IDord-0c054855ed7141da9368af0ad6b08622
Source noteuspto-grants-2000_04