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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401965Generated: October 27, 2026

Sodium Carbonate → HCID 136063621, compound

https://huagongshe.com/reaction/1401965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactanttert-butyl N-(4-chloropyridin-2-yl)carbamateHCID 1516418—
Reactant4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 56737703—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 136063621HCID 136063621—

Reaction Conditions

Temperature85 °C

Reaction Steps

4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (Preparation 212, 0.082 g, 0.000386 mol), tert-butyl (4-chloropyridin-2-yl)carbamate (0.0588 g, 0.000257 mol), anhydrous sodium carbonate (0.070 g, 0.000660 mol) and palladium (0) tetrakis(triphenylphosphine) (0.029 mg, 0.000025 mol) were suspended in 1,4-dioxane (3.0 ml) and water (1.0 ml). The suspension was stirred at 85° C. for 16 hours before cooling to room temperature. The reaction was diluted with ethyl acetate (10 ml) and organic phase was washed with saturated aqueous sodium bicarbonate solution (2×10.0 ml), dried over sodium sulphate, filtered and concentrated in vacuo. Purification by ISCO™ (12 g SiO2) eluting with ethyl acetate:heptane (gradient 0:1 to 3:7, by volume) afforded the title compound as a solid, 41 mg, 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-4f9a3b4e26ee4bb0bacf1bc41f096144
Source noteuspto-grants-2014_12