HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Ethoxy-2,3-difluorophenyl)-5-but-1-enylselenophene → 2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Ethoxy-2,3-difluorophenyl)-5-but-1-enylselenophene | HCID 72290248 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenophene | HCID 59456300 | — |
Reaction Steps
2.30 g (6.22 mmol) of 2-(4-ethoxy-2,3-difluorophenyl)-5-but-1-enylselenophene are hydrogenated in 70 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 recrystallisation from n-heptane. 2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenophene is obtained as a colourless solid (m.p. 47° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304036B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-256a354663ba448cb85aae320f3dcfb0 |
| Source note | uspto-grants-2012_11 |