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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914552Generated: October 30, 2026

Diethyl Ether → 5-Pyridin-4-yl-thiophene-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1914552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantCesium carbonateHCID 10796—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
ReactantEthyl 5-bromothiophene-3-carboxylateHCID 15293216—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-Pyridin-4-yl-thiophene-3-carboxylic acid ethyl esterHCID 581102862.9%

Reaction Conditions

Temperature140 °C

Reaction Steps

5-Bromo-thiophene-3-carboxylic acid ethyl ester (5.26 mmol), 4-pyridylboronic acid (5.26 mmol), caesium carbonate (7.9 mmol) and palladium (0) tetrakis-triphenylphosphine (0.53 mmol) were dissolved in a mixture of water (10 mL), IMS (20 mL) and DME (50 mL). The reaction mixture was heated by microwave irradiation to 140° C. for 10 minutes, and then ether (100 mL) and water (20 mL) were added. The organic solution was washed with water, dried with anhydrous magnesium sulfate, filtered and the solvent evaporated to give brown oil. The residue was purified by flash chromatography on silica. The fractions containing the desired product were concentrated under vacuum to give the title compound (0.035 g) as an off-white solid. LCMS m/z 234.04 [M+H]+ R.T.=2.10 min. (Analytical Method 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614209B2
Source datasetuspto-grants-2013_12
ORD IDord-12ce94c540f24bc79b3d7d16fd6233ea
Source noteuspto-grants-2013_12