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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966074Generated: October 30, 2026

Sodium Carbonate → HCID 9978819, compound

https://huagongshe.com/reaction/966074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 11744563HCID 11744563—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 9978819HCID 997881950%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a reaction flask charged with 14.7 mg (0.013 mmol) of tetrakis(triphenylphosphine)palladium(0) in ethylene glycol dimethyl ether (2.5 mL) under nitrogen was added 125 mg (0.27 mmol) of the product from Example 6. The resulting yellow solution was stirred for 10 min before the addition of 41.0 mg (0.32 mmol) of 3-thiopheneboronic acid dissolved in ethanol (0.2 mL) and the subsequent addition of 0.27 mL (0.54 mmol) of a 2 M sodium carbonate aqueous solution. The reaction mixture was heated at 80° C. for ˜20 h and then cooled to room temperature. The liquid was separated from the solid residue, and the residue was rinsed with dichloromethane, which was subsequently combined with the isolated liquid. The solvent was evaporated, and the crude product was partitioned between brine (˜4 mL) and dichloromethane (˜4 mL). The organic layer was washed with additional brine, dried over magnesium sulfate, and filtered. The solvent was evaporated, and the residue was purified by column chromatography (hexane/ethyl acetate) to yield 55 mg (50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951882B2
Source datasetuspto-grants-2005_10
ORD IDord-af7eb4e7ff1b456c9d704c1a131b7ba5
Source noteuspto-grants-2005_10