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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242116Generated: October 31, 2026

1,4-Dioxane → HCID 59205179, compound

https://huagongshe.com/reaction/2242116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromopyridine-3-carbaldehydeHCID 11116740—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthyl AcetateHCID 8857—
ProductHCID 59205179HCID 59205179—

Reaction Steps

A flask was charged with 4-bromo-pyridine-3-carbaldehyde (93 mg, 0.5 mmol), 5-formal-2-methoxylphenelboronic acid (88 mg, 0.6 mmol), tetrakis(triphenylphosphine) palladium(0) (29 mg, 0.025 mmol), potassium phosphate (160 mg, 0.75 mmol) and 1,4-dioxane (5 mL). The reaction mixture was kept at 50° C. overnight. The reaction mixture was then diluted with ethyl acetate and washed with water then brine. The organic layer was dried over sodium sulfate, concentrated, and the residue purified by flash chromatography to yield 4-(5-formyl-2-methoxy-phenyl)-pyridine-3-carbaldehyde as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671065B2
Source datasetuspto-grants-2010_03
ORD IDord-a3e417c32dbf4a1fb541348b3f305221
Source noteuspto-grants-2010_03