HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-(4-bromo-2-methoxyphenyl)ethanone → 4'-Bromo-2'-methoxy-2-(phthalimido)acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-(4-bromo-2-methoxyphenyl)ethanone | HCID 22316779 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4'-Bromo-2'-methoxy-2-(phthalimido)acetophenone | HCID 59134863 | 73.9% |
Reaction Steps
A solution of compound 6d (43.5 g) in anhydrous DMF (150 mL) was cooled to 5° C. To this solution was added potassium phthalimide (26.1 g, 141 mmol). After 5 min the cooling bath was removed and the reaction was allowed to stir at RT for 3 hr. The solvent was evaporated under vacuum to provide a tan solid. The solid was rinsed with 4:1 DCM/methanol and then water. The filter cake was slurried in toluene and evaporated to dryness to afford 4′-bromo-2′-methoxy-2-(phthalimido)acetophenone (compound 6e, 39 g) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652035B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-1f0043050ad0428781eaed8d4909bcec |
| Source note | uspto-grants-2010_01 |