HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873394Generated: October 25, 2026
Sodium Carbonate → 2-(4-Ethoxy-2,3-difluorophenyl)selenophene
https://huagongshe.com/reaction/1873394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromoselenophene | HCID 137013 | — |
| Reactant | B-(4-Ethoxy-2,3-difluorophenyl)boronic acid | HCID 15135235 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 2-(4-Ethoxy-2,3-difluorophenyl)selenophene | HCID 59456301 | — |
Reaction Steps
A mixture of 45.0 g (0.21 mol) of 2-bromoselenophene, 52.0 g (0.26 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 20.0 g (17.3 mmol) of tetrakis(triphenylphosphine)palladium(0) and 600 ml of 2 N sodium carbonate soln. in 1100 ml of toluene/ethanol (1:1) is heated under reflux for 20 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)selenophene is obtained as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304036B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-b0d75b2282834822b4ffc49a3ff86c7a |
|---|
| Source note | uspto-grants-2012_11 |
|---|