HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383368Generated: October 31, 2026
2-(4-Bromophenyl)ethanol → 2-{2-[4-(2-Hydroxy-ethyl)phenyl]-vinyl}-isoindole-1,3-dione
https://huagongshe.com/reaction/2383368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-ethenyl- | HCID 77035 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-{2-[4-(2-Hydroxy-ethyl)phenyl]-vinyl}-isoindole-1,3-dione | HCID 67029145 | — |
Reaction Steps
To a solution of 2-(4-bromophenyl)ethanol (48.3 g) in acetonitrile (480 mL) was added diisopropylethylamine (46.6 g), N-vinylphthalimide (43.7 g) and tri-o-tolylphosphine (7.31 g) and the mixture was purged with nitrogen gas three times. Palladium acetate (2.7 g) was added and the mixture was stirred at 90° C. for 21 hr under nitrogen. The reaction was cooled and the precipitated product collected by filtration. The resulting solid was re-dissolved in dichloromethane and ethyl acetate and filtered through silica gel. The filtrate was concentrated in vacuo to give the title compound, 24 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08263623B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-18504441bd204a2089c41bc9ea38e454 |
|---|
| Source note | uspto-grants-2012_09 |
|---|