HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873393Generated: October 25, 2026
Sodium Carbonate → 2-(4-Ethoxy-2,3-difluorophenyl)selenophene
https://huagongshe.com/reaction/1873393
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Iodoselenophene | HCID 142183 | — |
| Reactant | B-(4-Ethoxy-2,3-difluorophenyl)boronic acid | HCID 15135235 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 2-(4-Ethoxy-2,3-difluorophenyl)selenophene | HCID 59456301 | — |
Reaction Steps
A mixture of 34.8 g (0.14 mol) of 2-iodoselenophene, 32.8 g (0.16 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 8.10 g (77.01 mmol) of tetrakis -(triphenylphosphine)palladium(0) and 300 ml of 2 N sodium carbonate soln. in 800 ml of toluene/ethanol (1:1) is heated under reflux for 23 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 2 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:EtOAc=15:1-10:1→5:1). Further purification is carried out by recrystallisation from n-heptane; 2-(4-ethoxy-2,3-difluorophenyl)selenophene is obtained as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304036B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-0762230a08e74588a5910f25485ffb77 |
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| Source note | uspto-grants-2012_11 |
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