Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744685Generated: October 25, 2026

Sodium Carbonate → HCID 69545801, compound

https://huagongshe.com/reaction/1744685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant1-(tert-Butyl) 3-ethyl 4-(((trifluoromethyl)sulfonyl)oxy)-5,6-dihydropyridine-1,3(2H)-dicarboxylateHCID 22228409—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthyl AcetateHCID 8857—
SolventToluene ethanolHCID 21863594—
ProductHCID 69545801HCID 6954580187.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A vigorously stirred suspension of the product of step C (1.00 g, 2.48 mmol), 4-fluorophenylboronic acid (0.382 g, 2.73 mmol) and [1,1′-bis(diphenylphosphino)-ferrocene)dichloropalladium(II) (0.102 g, 0.124 mmol) in toluene/ethanol (3:2; 24.0 mL) was degassed via three vacuum/nitrogen ingress cycles and then heated to approximately 80° C. Aqueous 2 M sodium carbonate (3.10 mL, 6.20 mmol) was added dropwise via syringe and the resulting mixture maintained at reflux overnight. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and filtered through celite®. The filtrate was poured into water and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. Purification of the residue by medium pressure liquid chromatography on silica gel (gradient elution; 0–15% ethyl acetate/hexanes as eluent) afforded the title compound as a colorless oil (0.762 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015235B2
Source datasetuspto-grants-2006_03
ORD IDord-a55ccc77b2344db498f31461fd5a3774
Source noteuspto-grants-2006_03