HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18542728, compound → HCID 18542622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18542728 | HCID 18542728 | — |
| Reactant | HCID 86595369 | HCID 86595369 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18542622 | HCID 18542622 | 99.9% |
Reaction Steps
To a suspension of [3-(3-cyanophenyl)-2-(E)-propenyl]ethyl carbonate (1.04 g) and N-[4-(1-t-butoxycarbonylpiperidin-4-yloxy)phenyl]ethanesulfonamide (1.15 g) in tetrahydrofuran (9 ml) were added tris(dibenzylideneacetone)palladium chloroform complex (0.077 g) and triphenylphosphine (0.039 g) and the mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated in vacuo. The residue was purified by chromatography on a silica gel column using dichloromethane/ethyl acetate=8/1 as an eluant to give the desired compound (1.57 g, yield quantitative) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06555556B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-38707e4d0a744d5fbcdeec451324f485 |
| Source note | uspto-grants-2003_04 |