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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873423Generated: October 26, 2026

Sodium Carbonate → 4-Selenophen-2-ylphenol

https://huagongshe.com/reaction/1873423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-IodoselenopheneHCID 142183—
Reactant(2-Hydroxyphenyl)boronic acidHCID 2773454—
CatalystHCID 178418397HCID 178418397—
Solventtert-Butyl methyl etherHCID 15413—
SolventToluene ethanolHCID 21863594—
Product4-Selenophen-2-ylphenolHCID 12612806—

Reaction Steps

A mixture of 27.9 g (0.11 mol) of 2-iodoselenophene, 15.0 g (0.11 mol) of 2-hydroxyphenylboronic acid, 6.8 g (5.88 mmol) of tetrakis(triphenylphosphine)palladium(0) and 235 ml of 2 N sodium carbonate soln. in 600 ml of toluene/ethanol (1:1) is heated under reflux for 19 h. The mixture is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with 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:MTBE=4:1→1:1). Further purification is carried out by digestion in cold n-heptane; 4-selenophen-2-ylphenol is obtained as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-0758f29e362d49169dbb883bb272b792
Source noteuspto-grants-2012_11