HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596710Generated: November 1, 2026
Tri-o-tolylphosphine → HCID 67580760, compound
https://huagongshe.com/reaction/1596710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2-ButenaMide, N,N-diethyl-, (E)- | HCID 5354453 | — |
| Reactant | HCID 21702602 | HCID 21702602 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67580760 | HCID 67580760 | — |
Reaction Steps
A solution of 2-[5-bromo-2-[2,6-difluorobenzyloxy)phenyl]-1-ethanol (14.07 g, 41.02 mmol) and N,N-diethylcrotonamide (8.68 g, 61.53 mmol) in 60 mL triethylamine in a thick-walled pyrex tube is degassed wish nitrogen for 15 minutes. Pd(OAc)2 (0.46 g, 2.05 mmol) and tri-o-tolylphosphine (1.25 g, 4.10 mmol) are placed into the tube, which is then sealed, and the mixture is heated to 100° for 5 hours. The mixture is diluted with EtOAc (400 mL), and white precipitate is filtered out. The filtrate is then washed with 1 N HCl (2×400 mL), H20 (1×100 mL) and brine (1×100 ni), dried over MgSO4, and concentrated in vacuo. Chromatography (silica, 3:1 EtOAc/hexane) gives (E)-3-[4-(2,6-difluorobenzyloxy)-3-(2-hydroxyethyl)-phenyl]-2-butenoic acid diethy amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06291530B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-c1f1db60bfaa434794c8e7f4afa8bfaa |
|---|
| Source note | uspto-grants-2001_09 |
|---|