HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004297Generated: October 30, 2026
Potassium Carbonate → HCID 54255487, compound
https://huagongshe.com/reaction/1004297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54554919 | HCID 54554919 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54255487 | HCID 54255487 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06048861 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-0c054855ed7141da9368af0ad6b08622 |
|---|
| Source note | uspto-grants-2000_04 |
|---|