HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-But-1-enyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene → 2-Butyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-But-1-enyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene | HCID 72290262 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Butyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene | HCID 59456270 | — |
Reaction Steps
2.40 g (5.72 mmol) of 2-but-1-enyl-5-(4′-ethyl-2,3-difluorobiphenyl-4-yl)-selenophene are hydrogenated in 25 ml of ethyl acetate, in the presence of Pd/C (5% of Pd) at atmospheric pressure and RT. The reaction soln. is filtered and concentrated to dryness, and the crude product is purified by column chromatography (SiO2, n-heptane:toluene=9:1). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-Butyl-5-(4′-ethyl-2,3-difluorobiphenyl-4-yl)selenophene is obtained as a colourless solid (m.p. 73° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304036B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-d4501e35a5b645d881d3747aa8b87b8a |
| Source note | uspto-grants-2012_11 |