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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873440Generated: November 2, 2026

Sodium Carbonate → HCID 59456280, compound

https://huagongshe.com/reaction/1873440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromotelluropheneHCID 143604—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
SolventToluene ethanolHCID 21863594—
ProductHCID 59456280HCID 59456280—

Reaction Steps

A mixture of 10.0 g (38.7 mmol) of 2-bromotellurophene, 8.0 g (39.6 mmol) of 4-ethoxy-2,3-difluorophenylboronic acid, 3.5 g (3.0 mmol) of tetrakis-(triphenylphosphine)palladium(0) and 100 ml of 2 N sodium carbonate soln. in 200 ml of toluene/ethanol (1:1) is heated under reflux for 1.5 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with sat. sodium hydrogencarbonate soln., 1 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=3:2). Further purification is carried out by recrystallisation from ethanol; 2-(4-ethoxy-2,3-difluorophenyl)tellurophene is obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-1018220a9c224507b8c78d8d6affab89
Source noteuspto-grants-2012_11