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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967032Generated: October 30, 2026

Ethanol → HCID 86597234, compound

https://huagongshe.com/reaction/967032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3,4-Dimethoxyphenylboronic acidHCID 2734702—
ReactantHCID 23395706HCID 23395706—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86597234HCID 8659723469.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A quantity of 0.25 g (1.0 mmoles, 1 eq) of 6-bromo-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide and 0.28 g (1.5 mmoles, 1.5 eq) of 3,4-dimethoxyphenyl boronic acid are added in 20 mL of ethylene glycol dimethyl ether with 2 ml of ethanol and 2 ml of 2 M Na2CO3. The mixture is purged with N2 for 20 minutes, and then 57 mg (0.05 mmoles, 0.05 eq) of Tris (dibenzylideneacetone)-dipalladium (0) is added. The reaction is heated at 80° C. for 6 hours. At that time there is no starting material shown on TLC. The reaction is filtered through Celite and the solvent is removed. The residue is taken in ethyl acetate, washed with brine, dried over Na2SO4 and concentrated to afford 6-(3,4-dimethoxy-phenyl)-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide as a yellowish oil (0.21 g, 69%), which is used in the next step without purification. Analysis: MS (LC-MS): Calculated for C16H18N2O4 302.33, found 303.39 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953801B2
Source datasetuspto-grants-2005_10
ORD IDord-b7456821c01244abb3e0cf217d9638c7
Source noteuspto-grants-2005_10